A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406911



Internal ID21064464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3589802..3591143hg38UCSC Ensembl
chr6:3590036..3591377hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg381342
hg191342
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141733
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406911
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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