A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546923



Internal ID16334332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:102658247..102802203hg38UCSC Ensembl
Innerchr1:103123803..103267759hg19UCSC Ensembl
Innerchr1:102896391..103040347hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38143957
hg19143957
hg18143957
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv719701
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546923
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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