A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5928101



Internal ID22703336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:67436078..67436220hg38UCSC Ensembl
chr17:65432194..65432336hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17383568
Samples
Known GenesPITPNC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5928101
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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