A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5928812



Internal ID22704057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34215840..34216057hg38UCSC Ensembl
chr14:34685046..34685263hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg38218
hg19218
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17384702
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5928812
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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