A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17359059



Internal ID22584728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:112572592..112572592hg38UCSC Ensembl
chr12:113010396..113010396hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg38226
hg19226
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5973927
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17359059
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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