A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593896



Internal ID16381305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:29719135..29754407hg38UCSC Ensembl
Innerchr4:29720757..29756029hg19UCSC Ensembl
Innerchr4:29329855..29365127hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3835273
hg1935273
hg1835273
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv995195
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593896
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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