A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521700



Internal ID15102307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:43505454..43621909hg38UCSC Ensembl
Innerchr21:44925334..45041790hg19UCSC Ensembl
Innerchr21:43749762..43866218hg18UCSC Ensembl
Innerchr21:43749762..43866218hg17UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38116456
hg19116457
hg18116457
hg17116457
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698323
Samples
Known GenesHSF2BP, MIR6070
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521700
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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