A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695364



Internal ID15432016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:44375883..44379021hg38UCSC Ensembl
Innerchr22:44771763..44774901hg19UCSC Ensembl
Innerchr22:43150427..43153565hg18UCSC Ensembl
Innerchr22:43092300..43095438hg17UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg383139
hg193139
hg183139
hg173139
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517953
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695364
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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