A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv944872



Internal ID15892142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10420709..10475137hg38UCSC Ensembl
Innerchr21:11037320..11091748hg19UCSC Ensembl
Innerchr21:10059191..10113619hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg3854429
hg1954429
hg1854429
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586980
Supporting Variants
Samples
Known GenesBAGE, BAGE2, BAGE3, BAGE4, BAGE5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv944872
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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