A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214533



Internal ID20781574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:116798496..116950065hg38UCSC Ensembl
chr6:117119659..117271228hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg38151570
hg19151570
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6610828
Supporting Variants
Samples
Known GenesGPRC6A, RFX6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214533
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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