A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152192



Internal ID15873508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:44355905..44367919hg38UCSC Ensembl
Innerchr22:44751785..44763799hg19UCSC Ensembl
Innerchr22:43130449..43142463hg18UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3812015
hg1912015
hg1812015
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589105
Supporting Variants
SamplesHGDP00220
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152192
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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