A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17375901



Internal ID22601570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:97532799..97599526hg38UCSC Ensembl
chr15:98076029..98142756hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3866728
hg1966728
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5938544
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17375901
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