A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178066



Internal ID20745106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:50433796..51355774hg38UCSC Ensembl
chr15:50725993..51647971hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38921979
hg19921979
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6499738
Supporting Variants
Samples
Known GenesAP4E1, CYP19A1, DCAF13P3, GLDN, MIR4713, SPPL2A, TNFAIP8L3, TRPM7, USP50, USP8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178066
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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