A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217059



Internal ID20784099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167651363..167651929hg38UCSC Ensembl
chr6:168052043..168052609hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38567
hg19567
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6615726
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217059
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.94846


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