A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589337



Internal ID18540932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:17577691..17682315hg38UCSC Ensembl
Innerchr22:18058736..18165081hg19UCSC Ensembl
Innerchr22:16438736..16545081hg18UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38104625
hg19106346
hg18106346
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1064931
Supporting Variants
Samples
Known GenesATP6V1E1, BCL2L13, SLC25A18
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3589337
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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