A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546664



Internal ID16334073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:80373593..80443732hg38UCSC Ensembl
Innerchr1:80839278..80909417hg19UCSC Ensembl
Innerchr1:80611866..80682005hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3870140
hg1970140
hg1870140
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv342n54
Supporting Variantsnssv1173042
Samples1780862001_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546664
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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