A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593491



Internal ID16380900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:5733576..5780257hg38UCSC Ensembl
Innerchr4:5735303..5781984hg19UCSC Ensembl
Innerchr4:5786204..5832885hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3846682
hg1946682
hg1846682
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8932n54
Supporting Variantsnssv1152591
SamplesNINDS_36
Known GenesEVC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593491
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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