A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv719766



Internal ID16013722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:103582270..103591836hg38UCSC Ensembl
Innerchr1:104124892..104134458hg19UCSC Ensembl
Innerchr1:103926415..103935981hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg389567
hg199567
hg189567
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546982
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)nssv719766
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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