A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3733078



Internal ID18684673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:22196761..22247403hg38UCSC Ensembl
Innerchr22:22551161..22601814hg19UCSC Ensembl
Innerchr22:20881161..20931814hg18UCSC Ensembl
Cytoband22q11.22
Allele length
AssemblyAllele length
hg3850643
hg1950654
hg1850654
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1062771
Supporting Variants
Samples
Known GenesVPREB1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3733078
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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