A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695625



Internal ID15432277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:17775616..17780502hg38UCSC Ensembl
Innerchr22:18258382..18263268hg19UCSC Ensembl
Innerchr22:16638382..16643268hg18UCSC Ensembl
Innerchr22:16632936..16637822hg17UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg384887
hg194887
hg184887
hg174887
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518202
Supporting Variants
Samples
Known GenesLINC00528
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695625
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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