A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191417



Internal ID20758457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:118653429..118788326hg38UCSC Ensembl
chr12:119091234..119226131hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg38134898
hg19134898
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6476558
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191417
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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