A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17703623



Internal ID127289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:91294642..91294693hg38UCSC Ensembl
chr15:91837872..91837923hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5428312
Supporting Variants
Samples
Known GenesSV2B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17703623
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.004059


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