A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430901



Internal ID21088454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:77493246..77864833hg38UCSC Ensembl
chr8:78405482..78777068hg19UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg38371588
hg19371587
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18170398
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430901
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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