A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2795391



Internal ID21240729
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 StatusM
Merged Variants
Supporting Variantsnssv13687242
Samples
Known GenesADAMTSL3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2795391
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer