A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17711469



Internal ID135135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:11971283..11977083hg38UCSC Ensembl
chr17:11874600..11880400hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg385801
hg195801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6144351
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17711469
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.012766


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