A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352592



Internal ID21010145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:21678001..22101000hg38UCSC Ensembl
chr2:21900873..22323872hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38423000
hg19423000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085789
Samples
Known GenesLOC645949
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352592
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