A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17381830



Internal ID22439700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70877301..70882750hg38UCSC Ensembl
chr15:71169640..71175089hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg385450
hg195450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5940506
Supporting Variants
Samples
Known GenesLRRC49, THAP10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17381830
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