A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18085426



Internal ID20652466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:212424601..212426400hg38UCSC Ensembl
chr2:213289325..213291124hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6346350
Supporting Variants
Samples
Known GenesERBB4, MIR548F2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18085426
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00108


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