A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15176350



Internal ID21315146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:62039557..62039784hg38UCSC Ensembl
chr18:59706790..59707017hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38228
hg19228
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3931623
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15176350
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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