A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187921



Internal ID20754961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:31133611..31134935hg38UCSC Ensembl
chr15:31425814..31427138hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg381325
hg191325
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6495933
Supporting Variants
Samples
Known GenesTRPM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187921
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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