A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699930



Internal ID15436582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:69471312..69477780hg38UCSC Ensembl
Innerchr10:71231068..71237536hg19UCSC Ensembl
Innerchr10:70901074..70907542hg18UCSC Ensembl
Innerchr10:70901074..70907542hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg386469
hg196469
hg186469
hg176469
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524063
Supporting Variants
Samples
Known GenesTSPAN15
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699930
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer