A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703201



Internal ID15439853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:49362499..49377131hg38UCSC Ensembl
Innerchr10:50570544..50585177hg19UCSC Ensembl
Innerchr10:50240550..50255183hg18UCSC Ensembl
Innerchr10:50240550..50255183hg17UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3814633
hg1914634
hg1814634
hg1714634
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526843
Supporting Variants
Samples
Known GenesDRGX
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703201
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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