A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18228932



Internal ID20795972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:68155869..68165803hg38UCSC Ensembl
chr7:67620856..67630790hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg389935
hg199935
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6605176
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18228932
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00117


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