A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18091655



Internal ID20658695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:97671096..97684287hg38UCSC Ensembl
chr2:98287559..98300750hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3813192
hg1913192
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6339694
Supporting Variants
Samples
Known GenesLINC01125
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18091655
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