A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520586



Internal ID15101193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:40373074..40383482hg38UCSC Ensembl
Innerchr21:41745001..41755409hg19UCSC Ensembl
Innerchr21:40666871..40677279hg18UCSC Ensembl
Innerchr21:40666871..40677279hg17UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3810409
hg1910409
hg1810409
hg1710409
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv672846, nssv684507
Samples
Known GenesDSCAM, DSCAM-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520586
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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