A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597261



Internal ID16384670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:14913260..14962478hg38UCSC Ensembl
Innerchr5:14913369..14962587hg19UCSC Ensembl
Innerchr5:14966369..15015587hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3849219
hg1949219
hg1849219
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1026065
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597261
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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