A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6417751



Internal ID21075304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:79088301..79090100hg38UCSC Ensembl
chr8:80000536..80002335hg19UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18171160
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6417751
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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