A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17606120



Internal ID21798167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:38988200..38988397hg38UCSC Ensembl
chr13:39562337..39562534hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6039906
Supporting Variants
Samples
Known GenesSTOML3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17606120
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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