A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17379202



Internal ID22437072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41320934..41321091hg38UCSC Ensembl
chr15:41613132..41613289hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5938052
Supporting Variants
Samples
Known GenesOIP5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17379202
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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