A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407968



Internal ID21065521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:162442193..162442729hg38UCSC Ensembl
chr5:161869199..161869735hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38537
hg19537
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18126710
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407968
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