A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1031982



Internal ID15885168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:120883645..121441072hg38UCSC Ensembl
Innerchr5:120219340..120776767hg19UCSC Ensembl
Innerchr5:120247239..120804666hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38557428
hg19557428
hg18557428
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv599606
Supporting Variants
Samples
Known GenesLOC102467226
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1031982
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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