A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587400



Internal ID16374809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:33858960..33883235hg38UCSC Ensembl
Innerchr21:35231264..35255539hg19UCSC Ensembl
Innerchr21:34153134..34177409hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3824276
hg1924276
hg1824276
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv946650
Samples
Known GenesITSN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587400
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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