A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545164



Internal ID16332573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:5053851..5113744hg38UCSC Ensembl
Innerchr1:5113911..5173804hg19UCSC Ensembl
Innerchr1:5013771..5073664hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3859894
hg1959894
hg1859894
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv64n54
Supporting Variantsnssv1173648, nssv708944
SamplesHGDP00529
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545164
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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