A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224701



Internal ID20791741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:32571459..32572093hg38UCSC Ensembl
chr7:32611071..32611705hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38635
hg19635
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6601087
Supporting Variants
Samples
Known GenesAVL9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224701
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0007


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