A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697942



Internal ID15087908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:61837610..62047927hg38UCSC Ensembl
Innerchr15:62129809..62340126hg19UCSC Ensembl
Innerchr15:59917101..60127418hg18UCSC Ensembl
Innerchr15:59917101..60127418hg17UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38210318
hg19210318
hg18210318
hg17210318
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521334
Supporting Variants
Samples
Known GenesVPS13C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697942
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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