A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17367782



Internal ID22593451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122633342..122633406hg38UCSC Ensembl
chr10:124392858..124392922hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5908873
Supporting Variants
Samples
Known GenesDMBT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17367782
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