A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6344905



Internal ID21002458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:185163501..185312400hg38UCSC Ensembl
chr2:186028228..186177127hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg38148900
hg19148900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18082498
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6344905
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