A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18023986



Internal ID20591026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43541316..43548891hg38UCSC Ensembl
chr15:43833514..43841089hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg387576
hg197576
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6509520
Supporting Variants
Samples
Known GenesPPIP5K1, RNU6-28P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18023986
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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