A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219261



Internal ID20786301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155344101..155346800hg38UCSC Ensembl
chr7:155136809..155139499hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg382700
hg192691
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6435234
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219261
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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