A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18024756



Internal ID20591796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:48927581..48951027hg38UCSC Ensembl
chr15:49219778..49243224hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3823447
hg1923447
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6512867
Supporting Variants
Samples
Known GenesSHC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18024756
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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