A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597961



Internal ID16385370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:45187816..45193643hg38UCSC Ensembl
Innerchr5:45187918..45193745hg19UCSC Ensembl
Innerchr5:45223675..45229502hg18UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg385828
hg195828
hg185828
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9743n54
Supporting Variantsnssv1029623
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597961
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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