A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6145081



Internal ID344286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:831111..899100hg38UCSC Ensembl
chr17:734351..802340hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3867990
hg1967990
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17710719
Samples
Known GenesNXN
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6145081
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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