A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598964



Internal ID16386373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:97276697..97370058hg38UCSC Ensembl
Innerchr5:96612401..96705762hg19UCSC Ensembl
Innerchr5:96638157..96731518hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3893362
hg1993362
hg1893362
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1038113
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598964
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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