A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527022



Internal ID15107629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:42257721..42259403hg38UCSC Ensembl
Innerchr21:43677831..43679513hg19UCSC Ensembl
Innerchr21:42550900..42552582hg18UCSC Ensembl
Innerchr21:42550900..42552582hg17UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg381683
hg191683
hg181683
hg171683
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703397
Samples
Known GenesABCG1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527022
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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