A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427018



Internal ID21084571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:63175701..63183200hg38UCSC Ensembl
chr8:64088260..64095759hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg387500
hg197500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218325
Samples
Known GenesYTHDF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427018
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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