A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498742



Internal ID20871955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:99870660..100276199hg38UCSC Ensembl
chr15:100410865..100816404hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38405540
hg19405540
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2649n223
Supporting Variantsnssv18187082
Samples
Known GenesADAMTS17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498742
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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