A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17605102



Internal ID21797149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:90736061..90736170hg38UCSC Ensembl
chr13:91388315..91388424hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6023592
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17605102
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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