A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411799



Internal ID21069352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11996627..11999451hg38UCSC Ensembl
chr6:11996860..11999684hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg382825
hg192825
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137991
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411799
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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