A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6032692



Internal ID21942035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89338498..89345950hg38UCSC Ensembl
chr15:89881729..89889181hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg387453
hg197453
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17601157
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6032692
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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