A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6022607



Internal ID21931950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:53427279..53432030hg38UCSC Ensembl
chr15:53719476..53724227hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg384752
hg194752
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17613983
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6022607
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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