A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15175815



Internal ID21314611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:24938770..24938821hg38UCSC Ensembl
chr18:22518734..22518785hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3948479
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15175815
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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