A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18025255



Internal ID20592295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:56889809..56893629hg38UCSC Ensembl
chr15:57182007..57185827hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg383821
hg193821
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6499448
Supporting Variants
Samples
Known GenesLOC145783
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18025255
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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