A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234366



Internal ID20801407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:32466301..32468800hg38UCSC Ensembl
chr7:32505913..32508412hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6611039
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234366
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00263


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