A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211452



Internal ID20778492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:175360701..175377500hg38UCSC Ensembl
chr3:175078490..175095289hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3816800
hg1916800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6374944
Supporting Variants
Samples
Known GenesMIR4789, NAALADL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211452
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00016


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