A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352199



Internal ID21009752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:224230074..224232401hg38UCSC Ensembl
chr2:225094791..225097118hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg382328
hg192328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4291n223
Supporting Variantsnssv18083761
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352199
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