A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025175



Internal ID21934518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39131478..39133878hg38UCSC Ensembl
chr17:37287731..37290131hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg382401
hg192401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17617827
Samples
Known GenesPLXDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025175
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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