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esv1803800

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:184,992

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 883 SVs from 90 studies. See in: genome view    
Remapped(Score: Perfect):167,885,682-168,070,673Question Mark
Overlapping variant regions from other studies: 883 SVs from 90 studies. See in: genome view    
Remapped(Score: Perfect):168,806,833-168,991,824Question Mark
Overlapping variant regions from other studies: 280 SVs from 29 studies. See in: genome view    
Submitted genomic169,043,408-169,228,399Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner Stop
esv1803800RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000004.12Chr4167,885,682167,888,672168,070,673
esv1803800RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4168,806,833168,809,823168,991,824
esv1803800Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000004.10Chr4169,043,408169,046,398169,228,399

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv4423722copy number gainNA12239Oligo aCGHProbe signal intensity12,430

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner Stop
essv4423722RemappedPerfectNC_000004.12:g.(16
7885682_167888672)
_(168070673_?)dup
GRCh38.p12First PassNC_000004.12Chr4167,885,682167,888,672168,070,673
essv4423722RemappedPerfectNC_000004.11:g.(16
8806833_168809823)
_(168991824_?)dup
GRCh37.p13First PassNC_000004.11Chr4168,806,833168,809,823168,991,824
essv4423722Submitted genomicNC_000004.10:g.(16
9043408_169046398)
_(169228399_?)dup
NCBI36 (hg18)NC_000004.10Chr4169,043,408169,046,398169,228,399

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

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