A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428386



Internal ID21085939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:62306101..62312700hg38UCSC Ensembl
chr8:63218660..63225259hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg386600
hg196600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18168613
Samples
Known GenesNKAIN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428386
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer