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nsv6147115

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,932

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 133 SVs from 30 studies. See in: genome view    
Submitted genomic63,528,073-63,536,004Question Mark
Overlapping variant regions from other studies: 133 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):63,755,207-63,763,138Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6147115Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr263,528,07363,536,004
nsv6147115RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr263,755,20763,763,138

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16914938mobile element deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16914938Submitted genomicNC_000002.12:g.635
28073_63536004del
GRCh38 (hg38)NC_000002.12Chr263,528,07363,536,004
nssv16914938RemappedPerfectNC_000002.11:g.637
55207_63763138del
GRCh37.p13First PassNC_000002.11Chr263,755,20763,763,138

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv169149380.008526404
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