A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17724830



Internal ID148496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:56997866..56997917hg38UCSC Ensembl
chr17:55075227..55075278hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5423424
Supporting Variants
Samples
Known GenesSCPEP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17724830
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.011083


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