A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17714231



Internal ID137897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68628241..68648252hg38UCSC Ensembl
chr17:66624382..66644393hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3820012
hg1920012
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6145685
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17714231
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000937


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