A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426657



Internal ID21084210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:34327604..34328128hg38UCSC Ensembl
chr8:34185122..34185646hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38525
hg19525
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166699
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426657
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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