A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18027304



Internal ID20594344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92571116..92575257hg38UCSC Ensembl
chr15:93114346..93118487hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg384142
hg194142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6510007
Supporting Variants
Samples
Known GenesLINC00930
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18027304
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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