A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18024166



Internal ID20591206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39383745..39416251hg38UCSC Ensembl
chr15:39675946..39708452hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3832507
hg1932507
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6496408
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18024166
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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