A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546655



Internal ID16334064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:80055694..80097615hg38UCSC Ensembl
Innerchr1:80521379..80563300hg19UCSC Ensembl
Innerchr1:80293967..80335888hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3841922
hg1941922
hg1841922
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv339n54
Supporting Variantsnssv718339
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546655
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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