A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598767



Internal ID16386176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:82767349..82768107hg38UCSC Ensembl
Innerchr5:82063168..82063926hg19UCSC Ensembl
Innerchr5:82098924..82099682hg18UCSC Ensembl
Cytoband5q14.2
Allele length
AssemblyAllele length
hg38759
hg19759
hg18759
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1035326
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598767
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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