A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv680834



Internal ID15070800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:65392195..65401218hg38UCSC Ensembl
Innerchr15:65684533..65693556hg19UCSC Ensembl
Innerchr15:63471586..63480609hg18UCSC Ensembl
Innerchr15:63471586..63480609hg17UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg389024
hg199024
hg189024
hg179024
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515939
Supporting Variants
Samples
Known GenesIGDCC4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv680834
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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