A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15747296



Internal ID21389531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:61228513..61229303hg38UCSC Ensembl
chr15:61520712..61521502hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38791
hg19791
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4432239
Supporting Variants
SamplesNB09
Known GenesRORA
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15747296
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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