A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6394191



Internal ID21051744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:100856517..100856750hg38UCSC Ensembl
chr4:101777674..101777907hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38234
hg19234
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209431
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6394191
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