A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6348459



Internal ID21006012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:31976305..31978114hg38UCSC Ensembl
chr2:32201374..32203183hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg381810
hg191810
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085289
Samples
Known GenesMEMO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6348459
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