A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17359932



Internal ID22585601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18076345..18078565hg38UCSC Ensembl
chr11:18097892..18100112hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg382221
hg192221
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5921401
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17359932
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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