A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6084924



Internal ID21994157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83695228..83695228hg38UCSC Ensembl
chr15:84363980..84363980hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38425
hg19425
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609992
Samples
Known GenesADAMTSL3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6084924
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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