A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv946771



Internal ID16240727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:38744120..38780448hg38UCSC Ensembl
Innerchr21:40116044..40152372hg19UCSC Ensembl
Innerchr21:39037914..39074242hg18UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3836329
hg1936329
hg1836329
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv587475
Supporting Variants
Samples
Known GenesLINC00114
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv946771
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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