A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18023952



Internal ID20590992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42601201..42601900hg38UCSC Ensembl
chr15:42893399..42894098hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6508021
Supporting Variants
Samples
Known GenesSTARD9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18023952
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.07871


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