A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv956711



Internal ID16250667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:37352919..37353691hg38UCSC Ensembl
Innerchr22:37748959..37749731hg19UCSC Ensembl
Innerchr22:36078905..36079677hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38773
hg19773
hg18773
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589001
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv956711
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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