A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6613191



Internal ID20986262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:117064563..117072859hg38UCSC Ensembl
chr6:117385726..117394022hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg388297
hg198297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137211
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6613191
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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