A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6613968



Internal ID20987039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:163593803..163611180hg38UCSC Ensembl
chr6:164014835..164032212hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3817378
hg1917378
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18142265
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6613968
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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