A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497120



Internal ID20870324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83915613..83984104hg38UCSC Ensembl
chr15:84584365..84652856hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3868492
hg1968492
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187891
Samples
Known GenesADAMTSL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497120
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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