A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546860



Internal ID16334269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:95831382..95888421hg38UCSC Ensembl
Innerchr1:96296938..96353977hg19UCSC Ensembl
Innerchr1:96069526..96126565hg18UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3857040
hg1957040
hg1857040
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv719621
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546860
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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