A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035786



Internal ID21945129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74791265..74794755hg38UCSC Ensembl
chr15:75083606..75087096hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg383491
hg193491
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17601130
Samples
Known GenesCSK
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035786
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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