A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6351372



Internal ID21008925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:86687950..86701087hg38UCSC Ensembl
chr2:86915073..86928210hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg3813138
hg1913138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18091774
Samples
Known GenesRNF103-CHMP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6351372
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