A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17393138



Internal ID22451008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:101562002..101564767hg38UCSC Ensembl
chr3:101280846..101283611hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg382766
hg192766
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5893265
Supporting Variants
Samples
Known GenesTRMT10C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17393138
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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