A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424558



Internal ID21082111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:116029601..116040800hg38UCSC Ensembl
chr8:117041826..117053025hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3811200
hg1911200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18163117
Samples
Known GenesLINC00536
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424558
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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