A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431261



Internal ID21088814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:79178711..79248001hg38UCSC Ensembl
chr8:80090946..80160236hg19UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg3869291
hg1969291
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7395n223
Supporting Variantsnssv18171178
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431261
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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