A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17701973



Internal ID125639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:36899366..36899417hg38UCSC Ensembl
chr15:37191567..37191618hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5420619
Supporting Variants
Samples
Known GenesMEIS2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17701973
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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