A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370179



Internal ID21027732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:32360901..32366400hg38UCSC Ensembl
chr4:32362523..32368022hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg385500
hg195500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212877
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370179
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