A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695157



Internal ID15431809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:47171101..47171844hg38UCSC Ensembl
Innerchr22:47566744..47567487hg19UCSC Ensembl
Innerchr22:45945408..45946151hg18UCSC Ensembl
Innerchr22:45887263..45888006hg17UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38744
hg19744
hg18744
hg17744
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515802
Supporting Variants
Samples
Known GenesTBC1D22A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695157
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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