A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1035788



Internal ID15542288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:86791814..86821896hg38UCSC Ensembl
Innerchr5:86087631..86117713hg19UCSC Ensembl
Innerchr5:86123387..86153469hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3830083
hg1930083
hg1830083
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv598840
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1035788
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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