A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18235671



Internal ID20802711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2500131..2523937hg38UCSC Ensembl
chr7:2539765..2563571hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3823807
hg1923807
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6613339
Supporting Variants
Samples
Known GenesLFNG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18235671
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