A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18025929



Internal ID20592969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52738669..52744783hg38UCSC Ensembl
chr15:53030866..53036980hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg386115
hg196115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6503635
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18025929
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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