A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595802



Internal ID16383211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:156447839..156520489hg38UCSC Ensembl
Innerchr4:157368991..157441641hg19UCSC Ensembl
Innerchr4:157588441..157661091hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3872651
hg1972651
hg1872651
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1009754
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595802
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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