A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523629



Internal ID8417904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:36283012..36288308hg38UCSC Ensembl
Innerchr22:36679058..36684354hg19UCSC Ensembl
Innerchr22:35009004..35014300hg18UCSC Ensembl
Innerchr22:35003558..35008854hg17UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg385297
hg195297
hg185297
hg175297
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699428
Samples
Known GenesMIR6819, MYH9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523629
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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