A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv957153



Internal ID16251109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:42405493..42420973hg38UCSC Ensembl
Innerchr22:42801499..42816979hg19UCSC Ensembl
Innerchr22:41131443..41146923hg18UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3815481
hg1915481
hg1815481
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589070
Supporting Variants
Samples
Known GenesNFAM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv957153
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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