A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18027707



Internal ID20594747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:99204703..99306705hg38UCSC Ensembl
chr15:99744908..99846910hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38102003
hg19102003
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6501350
Supporting Variants
Samples
Known GenesHSP90B2P, LRRC28, TTC23
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18027707
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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