A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023469



Internal ID18766002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:156611368..156645912hg38UCSC Ensembl
Innerchr7:156404062..156438606hg19UCSC Ensembl
Innerchr7:156096823..156131367hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3834545
hg1934545
hg1834545
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3674705
Samples
Known GenesC7orf13, RNF32
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023469
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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