A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18207008



Internal ID20774048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:707603..905717hg38UCSC Ensembl
chr2:707603..901403hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38198115
hg19193801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6321585
Supporting Variants
Samples
Known GenesLINC01115
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18207008
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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