A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3600886



Internal ID18899167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:38890960..38924873hg38UCSC Ensembl
Innerchr22:39286965..39320878hg19UCSC Ensembl
Innerchr22:37616911..37650824hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3833914
hg1933914
hg1833914
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1066042
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)nssv3600886
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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