A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418215



Internal ID21075768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:98219188..98227676hg38UCSC Ensembl
chr8:99231416..99239904hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg388489
hg198489
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173841
Samples
Known GenesNIPAL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418215
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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