A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399741



Internal ID21057294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11165856..11175031hg38UCSC Ensembl
chr6:11166089..11175264hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg389176
hg199176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18135422
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399741
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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