A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005826



Internal ID18748357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:6682766..7004828hg38UCSC Ensembl
Innerchr3:6724453..7046515hg19UCSC Ensembl
Innerchr3:6699453..7021515hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38322063
hg19322063
hg18322063
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4674n100
Supporting Variantsnssv3591828
Samples
Known GenesGRM7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1005826
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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