A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6336587



Internal ID20994140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:33479054..33481299hg38UCSC Ensembl
chr2:33704121..33706366hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg382246
hg192246
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085949
Samples
Known GenesRASGRP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6336587
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