A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6037753



Internal ID21947096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39221769..39298075hg38UCSC Ensembl
chr15:39513970..39590276hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3876307
hg1976307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17604625
Samples
Known GenesC15orf54
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6037753
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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