A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219010



Internal ID20786050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:5100877..5175446hg38UCSC Ensembl
chr7:5140508..5215077hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3874570
hg1974570
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6619945
Supporting Variants
Samples
Known GenesZNF890P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219010
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