A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17354012



Internal ID22579681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:12975167..12985716hg38UCSC Ensembl
chr11:12996714..13007263hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3810550
hg1910550
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5909845
Supporting Variants
Samples
Known GenesLINC00958
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17354012
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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