A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607928



Internal ID20980999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167781677..167785689hg38UCSC Ensembl
chr6:168182357..168186369hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg384013
hg194013
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139296
Samples
Known GenesC6orf123
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607928
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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