U.S. flag

An official website of the United States government

esv3890983

  • Variant Calls:2
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:76,618

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1617 SVs from 96 studies. See in: genome view    
Remapped(Score: Perfect):162,281,502-162,358,119Question Mark
Overlapping variant regions from other studies: 1617 SVs from 96 studies. See in: genome view    
Remapped(Score: Perfect):162,702,534-162,779,151Question Mark
Overlapping variant regions from other studies: 538 SVs from 28 studies. See in: genome view    
Submitted genomic162,622,524-162,699,141Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
esv3890983RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr6162,281,502162,303,215162,358,119162,358,119
esv3890983RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6162,702,534162,724,247162,779,151162,779,151
esv3890983Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000006.10Chr6162,622,524162,644,237162,699,141162,699,141

Variant Call Information

Variant Call IDTypeMethodAnalysisCopy number
essv25789428copy number gainSNP arrayProbe signal intensity3
essv25778477copy number lossSNP arrayProbe signal intensity1

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv25789428RemappedPerfectNC_000006.12:g.(?_
162281502)_(162358
119_?)dup
GRCh38.p12First PassNC_000006.12Chr6162,281,502162,358,119
essv25778477RemappedPerfectNC_000006.12:g.(?_
162303215)_(162358
119_?)del
GRCh38.p12First PassNC_000006.12Chr6162,303,215162,358,119
essv25789428RemappedPerfectNC_000006.11:g.(?_
162702534)_(162779
151_?)dup
GRCh37.p13First PassNC_000006.11Chr6162,702,534162,779,151
essv25778477RemappedPerfectNC_000006.11:g.(?_
162724247)_(162779
151_?)del
GRCh37.p13First PassNC_000006.11Chr6162,724,247162,779,151
essv25789428Submitted genomicNC_000006.10:g.(?_
162622524)_(162699
141_?)dup
NCBI36 (hg18)NC_000006.10Chr6162,622,524162,699,141
essv25778477Submitted genomicNC_000006.10:g.(?_
162644237)_(162699
141_?)del
NCBI36 (hg18)NC_000006.10Chr6162,644,237162,699,141

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

Support Center