A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589103



Internal ID16376512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:44261855..44311836hg38UCSC Ensembl
Innerchr22:44657735..44707716hg19UCSC Ensembl
Innerchr22:42989068..43039049hg18UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3849982
hg1949982
hg1849982
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv957185
Samples
Known GenesKIAA1644
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589103
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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