A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18023903



Internal ID20590943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41689793..41694719hg38UCSC Ensembl
chr15:41981991..41986917hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg384927
hg194927
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6497881
Supporting Variants
Samples
Known GenesMGA, MIR626
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18023903
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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