A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17560133



Internal ID21884488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:3613621..3614234hg38UCSC Ensembl
chr7:3653253..3653866hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg38614
hg19614
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6005835
Supporting Variants
Samples
Known GenesSDK1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17560133
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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