A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152897



Internal ID15855367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:25555425..25576647hg38UCSC Ensembl
Innerchr4:25557047..25578269hg19UCSC Ensembl
Innerchr4:25166145..25187367hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3821223
hg1921223
hg1821223
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593832
Supporting Variants
Samples1780862575_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152897
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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