A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397888



Internal ID21055441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:5566294..5584175hg38UCSC Ensembl
chr6:5566527..5584408hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3817882
hg1917882
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18145820
Samples
Known GenesFARS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397888
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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