A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17714737



Internal ID138403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76591945..76591996hg38UCSC Ensembl
chr17:74588027..74588078hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5416598
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17714737
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.085545


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