A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610828



Internal ID20983899
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 StatusM
Merged Variants
Supporting Variantsnssv18214533
Samples
Known GenesGPRC6A, RFX6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610828
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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