A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231682



Internal ID20798722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:95384062..95387983hg38UCSC Ensembl
chr7:95013374..95017295hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg383922
hg193922
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617003
Supporting Variants
Samples
Known GenesPON3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231682
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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