A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv529006



Internal ID15109613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:50112978..50113047hg38UCSC Ensembl
Innerchr15:50405175..50405244hg19UCSC Ensembl
Innerchr15:48192467..48192536hg18UCSC Ensembl
Innerchr15:48192467..48192536hg17UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3870
hg1970
hg1870
hg1770
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705715
Samples
Known GenesATP8B4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv529006
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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