A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021479



Internal ID19110697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:19324324..19445896hg38UCSC Ensembl
Innerchr7:19363947..19485519hg19UCSC Ensembl
Innerchr7:19330472..19452044hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38121573
hg19121573
hg18121573
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643252
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)nsv1021479
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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