A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17602918



Internal ID21794965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:95690973..95691199hg38UCSC Ensembl
chr13:96343227..96343453hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38227
hg19227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6031048
Supporting Variants
Samples
Known GenesDNAJC3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17602918
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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