A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595882



Internal ID16383291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:160917560..161034677hg38UCSC Ensembl
Innerchr4:161838712..161955829hg19UCSC Ensembl
Innerchr4:162058162..162175279hg18UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg38117118
hg19117118
hg18117118
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9345n54
Supporting Variantsnssv1010002
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595882
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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