A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1034610



Internal ID15887796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:69017241..69024667hg38UCSC Ensembl
Innerchr5:68313068..68320494hg19UCSC Ensembl
Innerchr5:68348824..68356250hg18UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg387427
hg197427
hg187427
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv598414
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)nssv1034610
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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