A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355185



Internal ID21012738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:145669062..145670445hg38UCSC Ensembl
chr2:146426630..146428013hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg381384
hg191384
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18078348
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355185
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