A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17350502



Internal ID22576171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63687503..63692653hg38UCSC Ensembl
chr11:63454975..63460125hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg385151
hg195151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5926445
Supporting Variants
Samples
Known GenesRTN3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17350502
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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