A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4743785



Internal ID20519775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100378669..100379003hg38UCSC Ensembl
chr14:100845006..100845340hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16261814
Samples
Known GenesWDR25
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4743785
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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