A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6147137



Internal ID346319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:2495561..2514492hg38UCSC Ensembl
chr17:2398855..2417786hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3818932
hg1918932
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17709970
Samples
Known GenesMETTL16
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6147137
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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