A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697900



Internal ID15434552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:17104551..17105581hg38UCSC Ensembl
Innerchr22:17585441..17586471hg19UCSC Ensembl
Innerchr22:15965441..15966471hg18UCSC Ensembl
Innerchr22:15959995..15961025hg17UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg381031
hg191031
hg181031
hg171031
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519563
Supporting Variants
Samples
Known GenesIL17RA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697900
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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