A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17611100



Internal ID21803147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:21161878..21167988hg38UCSC Ensembl
chr13:21736017..21742127hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg386111
hg196111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6026259
Supporting Variants
Samples
Known GenesSKA3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17611100
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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