A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403479



Internal ID21061032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11972568..11973349hg38UCSC Ensembl
chr6:11972801..11973582hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg38782
hg19782
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137955
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403479
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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