A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399260



Internal ID21056813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:83108063..83419637hg38UCSC Ensembl
chr6:83817782..84129356hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38311575
hg19311575
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18145320
Samples
Known GenesDOPEY1, ME1, PGM3, RWDD2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399260
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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