A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1035124



Internal ID15888310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:75052965..75053542hg38UCSC Ensembl
Innerchr5:74348790..74349367hg19UCSC Ensembl
Innerchr5:74384546..74385123hg18UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38578
hg19578
hg18578
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv598664
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)nssv1035124
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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