A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528842



Internal ID15109449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:24139262..24247641hg38UCSC Ensembl
Innerchr22:24535229..24643609hg19UCSC Ensembl
Innerchr22:22865229..22973609hg18UCSC Ensembl
Innerchr22:22859783..22968163hg17UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg38108380
hg19108381
hg18108381
hg17108381
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705519
Samples
Known GenesCABIN1, GGT5, SUSD2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528842
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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