A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18025151



Internal ID20592191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:50010001..50010900hg38UCSC Ensembl
chr15:50302198..50303097hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6500821
Supporting Variants
Samples
Known GenesATP8B4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18025151
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00021


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