A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527371



Internal ID15107978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:35621066..35648760hg38UCSC Ensembl
Innerchr7:35660676..35688370hg19UCSC Ensembl
Innerchr7:35627201..35654895hg18UCSC Ensembl
Innerchr7:35433916..35461610hg17UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3827695
hg1927695
hg1827695
hg1727695
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703803
Samples
Known GenesHERPUD2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527371
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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