A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405107



Internal ID21062660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25938390..25940202hg38UCSC Ensembl
chr6:25938618..25940430hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg381813
hg191813
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140720
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405107
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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