A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17353571



Internal ID22579240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18549716..18653623hg38UCSC Ensembl
chr10:18838645..18942552hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38103908
hg19103908
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5910512
Supporting Variants
Samples
Known GenesNSUN6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17353571
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