A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17356624



Internal ID22582293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:13906853..13907737hg38UCSC Ensembl
chr11:13928400..13929284hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38885
hg19885
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5910185
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17356624
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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