A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035575



Internal ID21944918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43191201..43191346hg38UCSC Ensembl
chr15:43483399..43483544hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600890
Samples
Known GenesCCNDBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035575
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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