A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17610641



Internal ID21802688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74837505..74837556hg38UCSC Ensembl
chr15:75129846..75129897hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6023279
Supporting Variants
Samples
Known GenesULK3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17610641
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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