A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5934667



Internal ID22709997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:84409895..84410179hg38UCSC Ensembl
chr14:84876239..84876523hg19UCSC Ensembl
Cytoband14q31.2
Allele length
AssemblyAllele length
hg38285
hg19285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17386234
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5934667
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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