A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424404



Internal ID21081957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:110748567..110760917hg38UCSC Ensembl
chr8:111760796..111773146hg19UCSC Ensembl
Cytoband8q23.2
Allele length
AssemblyAllele length
hg3812351
hg1912351
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7456n223
Supporting Variantsnssv18163202
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424404
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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