A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035538



Internal ID21944881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72612560..72662539hg38UCSC Ensembl
chr15:72904901..72954880hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3849980
hg1949980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600615
Samples
Known GenesGOLGA6B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035538
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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