A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024392



Internal ID19113609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:47667425..47719378hg38UCSC Ensembl
Innerchr7:47707023..47758976hg19UCSC Ensembl
Innerchr7:47673548..47725501hg18UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg3851954
hg1951954
hg1851954
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6344n100
Supporting Variantsnssv3661243
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)nsv1024392
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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