A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022477



Internal ID19111695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:101322320..101492117hg38UCSC Ensembl
Innerchr7:100965601..101135398hg19UCSC Ensembl
Innerchr7:100752321..100922118hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38169798
hg19169798
hg18169798
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6537n100
Supporting Variantsnssv3655308, nssv3655307, nssv3755455, nssv3755454, nssv3655310, nssv3755456, nssv3655309
Samples
Known GenesCOL26A1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022477
Frequency
Sample Size11257
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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