A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4391134



Internal ID21379713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75237433..75237855hg38UCSC Ensembl
chr14:75704136..75704558hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38423
hg19423
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4n171
Supporting Variantsnssv15705796
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4391134
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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