A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546772



Internal ID16334181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:88017880..88579655hg38UCSC Ensembl
Innerchr1:88483563..89045338hg19UCSC Ensembl
Innerchr1:88256151..88817926hg18UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg38561776
hg19561776
hg18561776
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1173049
SamplesHGDP00647
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546772
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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