A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352529



Internal ID21010082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:164656891..164657309hg38UCSC Ensembl
chr2:165513401..165513819hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg38419
hg19419
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18079704
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352529
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