A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220481



Internal ID20787521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:154599601..154634400hg38UCSC Ensembl
chr7:154391311..154426110hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3834800
hg1934800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6424832
Supporting Variants
Samples
Known GenesDPP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220481
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00036


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