A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6408263



Internal ID21065816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:12304789..12324347hg38UCSC Ensembl
chr6:12305021..12324579hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg3819559
hg1919559
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137427
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6408263
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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