A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696277



Internal ID15432929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:57658997..57661366hg38UCSC Ensembl
Innerchr15:57951195..57953564hg19UCSC Ensembl
Innerchr15:55738487..55740856hg18UCSC Ensembl
Innerchr15:55738487..55740856hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg382370
hg192370
hg182370
hg172370
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518825
Supporting Variants
Samples
Known GenesGCOM1, MYZAP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696277
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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