A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3948025



Internal ID21368094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76347430..76347865hg38UCSC Ensembl
chr14:76813773..76814208hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38436
hg19436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15183175
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3948025
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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