A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546924



Internal ID16334333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:102711036..102794168hg38UCSC Ensembl
Innerchr1:103176592..103259724hg19UCSC Ensembl
Innerchr1:102949180..103032312hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3883133
hg1983133
hg1883133
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv385n54
Supporting Variantsnssv1173073
SamplesHGDP01347
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546924
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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