A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593987



Internal ID16381396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:36905679..36929802hg38UCSC Ensembl
Innerchr4:36907301..36931424hg19UCSC Ensembl
Innerchr4:36583696..36607819hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3824124
hg1924124
hg1824124
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv995863
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593987
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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