A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377526



Internal ID21035079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:42822437..42967664hg38UCSC Ensembl
chr4:42824454..42969681hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38145228
hg19145228
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213648
Samples
Known GenesGRXCR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377526
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