A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18026063



Internal ID20593103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:61010597..61011052hg38UCSC Ensembl
chr15:61302796..61303251hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38456
hg19456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6503934
Supporting Variants
Samples
Known GenesRORA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18026063
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00023


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