A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17497082



Internal ID22555016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:167297691..167302740hg38UCSC Ensembl
chr5:166724696..166729745hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg385050
hg195050
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5842170
Supporting Variants
Samples
Known GenesTENM2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17497082
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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