A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546853



Internal ID16334262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:94661907..94688723hg38UCSC Ensembl
Innerchr1:95127463..95154279hg19UCSC Ensembl
Innerchr1:94900051..94926867hg18UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3826817
hg1926817
hg1826817
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1173063
SamplesHGDP00921
Known GenesLINC01057
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546853
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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