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nsv5502567

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:11,232

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 158 SVs from 39 studies. See in: genome view    
Submitted genomic114,959,879-114,971,110Question Mark
Overlapping variant regions from other studies: 158 SVs from 39 studies. See in: genome view    
Remapped(Score: Perfect):116,719,638-116,730,869Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5502567Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10114,959,879114,971,110
nsv5502567RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10116,719,638116,730,869

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17039243deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17039243Submitted genomicNC_000010.11:g.114
959879_114971110de
l
GRCh38 (hg38)NC_000010.11Chr10114,959,879114,971,110
nssv17039243RemappedPerfectNC_000010.10:g.116
719638_116730869de
l
GRCh37.p13First PassNC_000010.10Chr10116,719,638116,730,869

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)
nssv17039243<0.00136404
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