A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380938



Internal ID21038491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:66564344..66593103hg38UCSC Ensembl
chr4:67430062..67458821hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3828760
hg1928760
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18120008
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380938
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer