A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4743464



Internal ID20519452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:38775044..38775176hg38UCSC Ensembl
chr17:36931297..36931429hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16291957
Samples
Known GenesPIP4K2B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4743464
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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