A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13686526



Internal ID21208383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40529729..40531389hg38UCSC Ensembl
chr15:40821928..40823588hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg381661
hg191661
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2794206
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13686526
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0625


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