A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18085601



Internal ID20652641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:25345625..25350745hg38UCSC Ensembl
chr2:25568494..25573614hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg385121
hg195121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6346099
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18085601
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