A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219026



Internal ID20786066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75738601..75742800hg38UCSC Ensembl
chr7:75367919..75372118hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg384200
hg194200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6615716
Supporting Variants
Samples
Known GenesHIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219026
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00491


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