A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18078518



Internal ID20645559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:155015166..155111417hg38UCSC Ensembl
chr2:155871678..155967929hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg3896252
hg1996252
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6348200
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18078518
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer