A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997822



Internal ID19157359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:163875341..164197870hg38UCSC Ensembl
Innerchr1:163844578..164167107hg19UCSC Ensembl
Innerchr1:162111202..162433731hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38322530
hg19322530
hg18322530
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3704810
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)nsv997822
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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