A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375710



Internal ID21033263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:121376601..121385300hg38UCSC Ensembl
chr4:122297756..122306455hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg388700
hg198700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210219
Samples
Known GenesQRFPR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375710
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