A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696871



Internal ID15433523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:26458475..26463976hg38UCSC Ensembl
Innerchr22:26854441..26859942hg19UCSC Ensembl
Innerchr22:25184441..25189942hg18UCSC Ensembl
Innerchr22:25178995..25184496hg17UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg385502
hg195502
hg185502
hg175502
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519472
Supporting Variants
Samples
Known GenesHPS4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696871
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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