A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389605



Internal ID21047158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:61764601..61769700hg38UCSC Ensembl
chr4:62630319..62635418hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg385100
hg195100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210907
Samples
Known GenesLPHN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389605
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