A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038696



Internal ID21948039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66386174..66386238hg38UCSC Ensembl
chr15:66678512..66678576hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17610455
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038696
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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