A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13687242



Internal ID21209096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83695229..83695229hg38UCSC Ensembl
chr15:84363981..84363981hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38454
hg19454
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2795391
Supporting Variants
Samples
Known GenesADAMTSL3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13687242
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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