A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419729



Internal ID21077282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:48904293..48907173hg38UCSC Ensembl
chr8:49816852..49819732hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg382881
hg192881
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167771
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419729
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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