A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18027286



Internal ID20594326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92217541..92557558hg38UCSC Ensembl
chr15:92760771..93100788hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38340018
hg19340018
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502480
Supporting Variants
Samples
Known GenesC15orf32, ST8SIA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18027286
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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