A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192157



Internal ID20759197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55971001..56009300hg38UCSC Ensembl
chr15:56263199..56301498hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3838300
hg1938300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6503527
Supporting Variants
Samples
Known GenesNEDD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192157
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00084


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