A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6433405



Internal ID21090958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:13646387..13832532hg38UCSC Ensembl
chr8:13503896..13690041hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38186146
hg19186146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18164493
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6433405
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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