A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6146119



Internal ID345324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15960292..15960572hg38UCSC Ensembl
chr17:15863606..15863886hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17711745
Samples
Known GenesADORA2B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6146119
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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