A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18024018



Internal ID20591058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51454557..51454827hg38UCSC Ensembl
chr15:51746754..51747024hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38271
hg19271
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514188
Supporting Variants
Samples
Known GenesDMXL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18024018
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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