A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1027969



Internal ID16321925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:24047731..24136065hg38UCSC Ensembl
Innerchr5:24047840..24136174hg19UCSC Ensembl
Innerchr5:24083597..24171931hg18UCSC Ensembl
Cytoband5p14.2
Allele length
AssemblyAllele length
hg3888335
hg1988335
hg1888335
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597605
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)nssv1027969
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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