A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153297



Internal ID15880523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:28763545..28870396hg38UCSC Ensembl
Innerchr5:28763652..28870503hg19UCSC Ensembl
Innerchr5:28799409..28906260hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg38106852
hg19106852
hg18106852
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597713
Supporting Variants
SamplesNINDS_222
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153297
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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