A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6034108



Internal ID21943451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64799168..64799249hg38UCSC Ensembl
chr15:65091367..65091448hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17614217
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6034108
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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