A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151831



Internal ID15531516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:23553438..23613578hg38UCSC Ensembl
Innerchr22:23895625..23955765hg19UCSC Ensembl
Innerchr22:22225625..22285765hg18UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3860141
hg1960141
hg1860141
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv588606
Supporting Variants
SamplesHGDP01155
Known GenesC22orf43, IGLL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151831
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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