A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv947141



Internal ID16241097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:41687463..41713669hg38UCSC Ensembl
Innerchr21:43107623..43133829hg19UCSC Ensembl
Innerchr21:41980692..42006898hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3826207
hg1926207
hg1826207
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv587560
Supporting Variants
Samples
Known GenesLINC00111, LINC00479
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv947141
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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