A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598835



Internal ID16386244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:86310631..86355216hg38UCSC Ensembl
Innerchr5:85606449..85651034hg19UCSC Ensembl
Innerchr5:85642205..85686790hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3844586
hg1944586
hg1844586
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9919n54
Supporting Variantsnssv1035783, nssv1035784
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598835
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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