A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399261



Internal ID21056814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:80701832..80707374hg38UCSC Ensembl
chr6:81411549..81417091hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg385543
hg195543
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18147309
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399261
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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