A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18023933



Internal ID20590973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42350281..42350807hg38UCSC Ensembl
chr15:42642479..42643005hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38527
hg19527
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6505068
Supporting Variants
Samples
Known GenesGANC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18023933
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00363


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