A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17560113



Internal ID21884468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:123677222..124027180hg38UCSC Ensembl
chr6:123998367..124348325hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38349959
hg19349959
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6019101
Supporting Variants
Samples
Known GenesNKAIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17560113
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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