A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595881



Internal ID16383290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:160917560..161014190hg38UCSC Ensembl
Innerchr4:161838712..161935342hg19UCSC Ensembl
Innerchr4:162058162..162154792hg18UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg3896631
hg1996631
hg1896631
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9345n54
Supporting Variantsnssv1153239
SamplesHGDP00955
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595881
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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