A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17497086



Internal ID22555020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:167690128..167695763hg38UCSC Ensembl
chr5:167117133..167122768hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg385636
hg195636
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5841854
Supporting Variants
Samples
Known GenesTENM2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17497086
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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