A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15182510



Internal ID21321306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:117320376..117320534hg38UCSC Ensembl
chr11:117191092..117191250hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3937860
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15182510
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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