A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18077289



Internal ID20644329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:142364112..142382194hg38UCSC Ensembl
chr2:143121681..143139763hg19UCSC Ensembl
Cytoband2q22.2
Allele length
AssemblyAllele length
hg3818083
hg1918083
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6343102
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18077289
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