A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026064



Internal ID21935407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83948202..83965648hg38UCSC Ensembl
chr15:84616954..84634400hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3817447
hg1917447
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17608312
Samples
Known GenesADAMTSL3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026064
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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