A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17357683



Internal ID22583352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:122112094..122112094hg38UCSC Ensembl
chr11:121982802..121982802hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg38249
hg19249
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5977300
Supporting Variants
Samples
Known GenesMIR100HG
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17357683
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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