A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595879



Internal ID16383288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:160917560..161006375hg38UCSC Ensembl
Innerchr4:161838712..161927527hg19UCSC Ensembl
Innerchr4:162058162..162146977hg18UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg3888816
hg1988816
hg1888816
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9345n54
Supporting Variantsnssv1153237, nssv1153236
SamplesHGDP01288, HGDP01310
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595879
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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