A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6040019



Internal ID21949362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42801161..42801316hg38UCSC Ensembl
chr15:43093359..43093514hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17611141
Samples
Known GenesTTBK2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6040019
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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