A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405034



Internal ID21062587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:68334004..68387211hg38UCSC Ensembl
chr6:69043896..69097103hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3853208
hg1953208
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18146345
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405034
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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