A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6402519



Internal ID21060072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:90518018..90518579hg38UCSC Ensembl
chr5:89813835..89814396hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38562
hg19562
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18134928
Samples
Known GenesLYSMD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6402519
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