A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17360679



Internal ID22586348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63479655..63485493hg38UCSC Ensembl
chr11:63247127..63252965hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg385839
hg195839
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5911540
Supporting Variants
Samples
Known GenesHRASLS5, MIR3680-1, MIR3680-2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17360679
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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