A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593782



Internal ID16381191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:19033985..19303323hg38UCSC Ensembl
Innerchr4:19035608..19304946hg19UCSC Ensembl
Innerchr4:18644706..18914044hg18UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg38269339
hg19269339
hg18269339
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153452
SamplesHGDP00161
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593782
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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