A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587932



Internal ID16375341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:45978497..45998397hg38UCSC Ensembl
Innerchr21:47398411..47418311hg19UCSC Ensembl
Innerchr21:46222839..46242739hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3819901
hg1919901
hg1819901
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7919n54
Supporting Variantsnssv949281
Samples
Known GenesCOL6A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587932
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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