A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598832



Internal ID16386241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:85815502..85853630hg38UCSC Ensembl
Innerchr5:85111320..85149448hg19UCSC Ensembl
Innerchr5:85147076..85185204hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3838129
hg1938129
hg1838129
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9918n54
Supporting Variantsnssv1035780
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598832
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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