A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434517



Internal ID21396519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:142201266..142207979hg38UCSC Ensembl
chr5:141580831..141587544hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg386714
hg196714
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15747378, nssv15746837, nssv15753879
SamplesBTQ038, BTQ055, BTQ016
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434517
Frequency
Sample Size15
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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