A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022047



Internal ID18764581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:12477851..12512521hg38UCSC Ensembl
Innerchr7:12517477..12552147hg19UCSC Ensembl
Innerchr7:12484002..12518672hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3834671
hg1934671
hg1834671
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6273n100
Supporting Variantsnssv3642971
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)nsv1022047
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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