A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526673



Internal ID15107280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:44291319..44303501hg38UCSC Ensembl
Innerchr21:45711202..45723384hg19UCSC Ensembl
Innerchr21:44535630..44547812hg18UCSC Ensembl
Innerchr21:44535630..44547812hg17UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3812183
hg1912183
hg1812183
hg1712183
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703005
Samples
Known GenesAIRE, PFKL
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526673
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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