A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545163



Internal ID16332572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:5053851..5110652hg38UCSC Ensembl
Innerchr1:5113911..5170712hg19UCSC Ensembl
Innerchr1:5013771..5070572hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3856802
hg1956802
hg1856802
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv64n54
Supporting Variantsnssv708941, nssv708943, nssv708942
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545163
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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