A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17714006



Internal ID137672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63588544..63588595hg38UCSC Ensembl
chr17:61665906..61665957hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38235
hg19235
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5419432
Supporting Variants
Samples
Known GenesDCAF7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17714006
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.014205


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