A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546891



Internal ID15987614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:101243196..101267549hg38UCSC Ensembl
Innerchr1:101708752..101733105hg19UCSC Ensembl
Innerchr1:101481340..101505693hg18UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg3824354
hg1924354
hg1824354
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv719667
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546891
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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