A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423574



Internal ID21081127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11399085..11474110hg38UCSC Ensembl
chr8:11256594..11331619hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3875026
hg1975026
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18163278
Samples
Known GenesC8orf12, FAM167A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423574
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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