A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590972



Internal ID16378381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:90215618..90342524hg38UCSC Ensembl
Innerchr3:90264768..90391674hg19UCSC Ensembl
Innerchr3:90347458..90474364hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg38126907
hg19126907
hg18126907
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8439n54
Supporting Variantsnssv967757
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590972
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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