A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595878



Internal ID16383287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:160916563..161006375hg38UCSC Ensembl
Innerchr4:161837715..161927527hg19UCSC Ensembl
Innerchr4:162057165..162146977hg18UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg3889813
hg1989813
hg1889813
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9345n54
Supporting Variantsnssv1153235
SamplesHGDP00785
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595878
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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