A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6145349



Internal ID344554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:83208900..83227133hg38UCSC Ensembl
chr17:81156669..81174902hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3818234
hg1918234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17715099
Samples
Known GenesFLJ43681
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6145349
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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