A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17494639



Internal ID22552570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:67598710..67653991hg38UCSC Ensembl
chr3:67649134..67704415hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3855282
hg1955282
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5837001
Supporting Variants
Samples
Known GenesSUCLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17494639
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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