A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505330



Internal ID20878598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100058266..100058365hg38UCSC Ensembl
chr15:100598471..100598570hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185727
Samples
Known GenesADAMTS17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505330
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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