A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909845



Internal ID22685055
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 StatusM
Merged Variants
Supporting Variantsnssv17354012
Samples
Known GenesLINC00958
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909845
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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