A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18025215



Internal ID20592255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:50893895..51071954hg38UCSC Ensembl
chr15:51186092..51364151hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38178060
hg19178060
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6507375
Supporting Variants
Samples
Known GenesAP4E1, DCAF13P3, TNFAIP8L3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18025215
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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