A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17502990



Internal ID22560931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166954710..166961355hg38UCSC Ensembl
chr6:167368198..167374843hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg386646
hg196646
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5844196
Supporting Variants
Samples
Known GenesRNASET2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17502990
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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