A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17712370



Internal ID136036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28623717..28623768hg38UCSC Ensembl
chr17:26950735..26950786hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38260
hg19260
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5416331
Supporting Variants
Samples
Known GenesKIAA0100
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17712370
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003278


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