A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412599



Internal ID21070152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:63296642..63297120hg38UCSC Ensembl
chr5:62592469..62592947hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg38479
hg19479
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18132560
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412599
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