A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17358117



Internal ID22583786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61364834..61365126hg38UCSC Ensembl
chr11:61132306..61132598hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5910842
Supporting Variants
Samples
Known GenesTMEM138
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17358117
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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