A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18083822



Internal ID20650862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:237161700..237162538hg38UCSC Ensembl
chr2:238070343..238071181hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38839
hg19839
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6344581
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18083822
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