A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525176



Internal ID15452469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:42298214..42299999hg38UCSC Ensembl
Innerchr22:42694220..42696005hg19UCSC Ensembl
Innerchr22:41024164..41025949hg18UCSC Ensembl
Innerchr22:41018718..41020503hg17UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg381786
hg191786
hg181786
hg171786
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701252
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525176
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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