A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17606516



Internal ID21798563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74798955..74799032hg38UCSC Ensembl
chr15:75091296..75091373hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6036212
Supporting Variants
Samples
Known GenesCSK
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17606516
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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