A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15750096



Internal ID21388327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:24323409..24324603hg38UCSC Ensembl
chr18:21903373..21904567hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg381195
hg191195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4432650
Supporting Variants
SamplesNB07
Known GenesOSBPL1A
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15750096
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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