A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv947347



Internal ID15894617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:41983779..42002416hg38UCSC Ensembl
Innerchr21:43403888..43422525hg19UCSC Ensembl
Innerchr21:42276957..42295594hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3818638
hg1918638
hg1818638
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv587623
Supporting Variants
Samples
Known GenesZBTB21
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv947347
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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