A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595470



Internal ID16382879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:133262495..133470040hg38UCSC Ensembl
Innerchr4:134183650..134391195hg19UCSC Ensembl
Innerchr4:134403100..134610645hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38207546
hg19207546
hg18207546
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1006915
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595470
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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