A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596946



Internal ID16384355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:6528784..6549055hg38UCSC Ensembl
Innerchr5:6528897..6549168hg19UCSC Ensembl
Innerchr5:6581897..6602168hg18UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3820272
hg1920272
hg1820272
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1023700
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596946
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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