A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527542



Internal ID15108149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:46595956..46607967hg38UCSC Ensembl
Innerchr21:48015869..48027880hg19UCSC Ensembl
Innerchr21:46840297..46852308hg18UCSC Ensembl
Innerchr21:46840297..46852308hg17UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3812012
hg1912012
hg1812012
hg1712012
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704003
Samples
Known GenesS100B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527542
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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