A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595731



Internal ID16383140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:151869428..151910157hg38UCSC Ensembl
Innerchr4:152790580..152831309hg19UCSC Ensembl
Innerchr4:153010030..153050759hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3840730
hg1940730
hg1840730
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153173
SamplesHGDP01007
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595731
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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