A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6391796



Internal ID21049349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:94311875..94322653hg38UCSC Ensembl
chr4:95233026..95243804hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg3810779
hg1910779
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215391
Samples
Known GenesHPGDS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6391796
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