A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18078140



Internal ID20645180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:144425201..144426900hg38UCSC Ensembl
chr2:145182768..145184467hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6355009
Supporting Variants
Samples
Known GenesZEB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18078140
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