A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016732



Internal ID19105949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:36682760..36723278hg38UCSC Ensembl
Innerchr7:36722365..36762883hg19UCSC Ensembl
Innerchr7:36688890..36729408hg18UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3840519
hg1940519
hg1840519
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643425
Samples
Known GenesAOAH
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016732
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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