A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225252



Internal ID20792292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:100078427..100082517hg38UCSC Ensembl
chr7:99676050..99680140hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg384091
hg194091
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6601568
Supporting Variants
Samples
Known GenesZNF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225252
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