A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2794790



Internal ID21240128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100058302..100058302hg38UCSC Ensembl
chr15:100598507..100598507hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13677812
Samples
Known GenesADAMTS17
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2794790
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