A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17608505



Internal ID21800552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:102137767..102137889hg38UCSC Ensembl
chr13:102790117..102790239hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6022274
Supporting Variants
Samples
Known GenesFGF14
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17608505
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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