A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17601192



Internal ID21793239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:74297464..74300007hg38UCSC Ensembl
chr13:74871601..74874144hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg382544
hg192544
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6038398
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17601192
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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