A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219323



Internal ID20786363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:24755801..24760800hg38UCSC Ensembl
chr7:24795420..24800419hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg385000
hg195000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6612703
Supporting Variants
Samples
Known GenesDFNA5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219323
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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