A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6145268



Internal ID344473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:67436112..67436221hg38UCSC Ensembl
chr17:65432228..65432337hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17714158
Samples
Known GenesPITPNC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6145268
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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