A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18024676



Internal ID20591716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49467088..49467816hg38UCSC Ensembl
chr15:49759285..49760013hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38729
hg19729
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514797
Supporting Variants
Samples
Known GenesFAM227B, FGF7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18024676
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00029


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