A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18023569



Internal ID20590609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:33063260..33069964hg38UCSC Ensembl
chr15:33355461..33362165hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg386705
hg196705
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6496187
Supporting Variants
Samples
Known GenesFMN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18023569
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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