A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17600461



Internal ID21792508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:74519452..74524648hg38UCSC Ensembl
chr13:75093589..75098785hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg385197
hg195197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6026465
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17600461
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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