A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426963



Internal ID21084516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:103132626..103133305hg38UCSC Ensembl
chr8:104144854..104145533hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38680
hg19680
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162533
Samples
Known GenesC8orf56
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426963
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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