A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025576



Internal ID19114794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:57638217..57960277hg38UCSC Ensembl
Innerchr7:57697923..58019983hg19UCSC Ensembl
Innerchr7:57701865..58023925hg18UCSC Ensembl
Cytoband7p11.1
Allele length
AssemblyAllele length
hg38322061
hg19322061
hg18322061
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6378n100
Supporting Variantsnssv3752980
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025576
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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