A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1000551



Internal ID15947821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:62837070..63259463hg38UCSC Ensembl
Innerchr4:63702788..64125181hg19UCSC Ensembl
Innerchr4:63385383..63807776hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38422394
hg19422394
hg18422394
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv594370
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1000551
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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