A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399331



Internal ID21056884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:68633062..68635384hg38UCSC Ensembl
chr6:69342954..69345276hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg382323
hg192323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143826
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399331
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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