A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596944



Internal ID16384353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:5840573..5857441hg38UCSC Ensembl
Innerchr5:5840686..5857554hg19UCSC Ensembl
Innerchr5:5893686..5910554hg18UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg3816869
hg1916869
hg1816869
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152994
Samples1798860565_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596944
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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