A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3734208



Internal ID19032489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:35501977..35530772hg38UCSC Ensembl
Innerchr22:35898024..35926819hg19UCSC Ensembl
Innerchr22:34227970..34256765hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3828796
hg1928796
hg1828796
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058946
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3734208
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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