A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18024757



Internal ID20591797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:48936380..48937026hg38UCSC Ensembl
chr15:49228577..49229223hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38647
hg19647
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6506315
Supporting Variants
Samples
Known GenesSHC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18024757
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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