A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421029



Internal ID21078582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:108223701..108224800hg38UCSC Ensembl
chr8:109235930..109237029hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162181
Samples
Known GenesEIF3E
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421029
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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