A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596263



Internal ID16383672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:176229811..176246589hg38UCSC Ensembl
Innerchr4:177150962..177167740hg19UCSC Ensembl
Innerchr4:177387956..177404734hg18UCSC Ensembl
Cytoband4q34.2
Allele length
AssemblyAllele length
hg3816779
hg1916779
hg1816779
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1017029
Samples
Known GenesASB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596263
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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