A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6353354



Internal ID21010907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:183195552..183196522hg38UCSC Ensembl
chr2:184060280..184061250hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg38971
hg19971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18081656
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6353354
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