A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv718372



Internal ID16012328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:81614025..81637239hg38UCSC Ensembl
Innerchr1:82079710..82102924hg19UCSC Ensembl
Innerchr1:81852298..81875512hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3823215
hg1923215
hg1823215
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546680
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv718372
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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