A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431880



Internal ID21089433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94830071..94831577hg38UCSC Ensembl
chr8:95842299..95843805hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg381507
hg191507
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18171831
Samples
Known GenesINTS8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431880
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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