A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594474



Internal ID16381883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:64641975..64669752hg38UCSC Ensembl
Innerchr4:65507693..65535470hg19UCSC Ensembl
Innerchr4:65190288..65218065hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3827778
hg1927778
hg1827778
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153144
Samples1780854495_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594474
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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