A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv667247



Internal ID15057213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:40265863..40303426hg38UCSC Ensembl
Innerchr15:40558064..40595627hg19UCSC Ensembl
Innerchr15:38345356..38382919hg18UCSC Ensembl
Innerchr15:38345356..38382919hg17UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3837564
hg1937564
hg1837564
hg1737564
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517541
Supporting Variants
Samples
Known GenesANKRD63, PAK6, PLCB2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv667247
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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