A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5932147



Internal ID22707440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:62145951..62151213hg38UCSC Ensembl
chr14:62612669..62617931hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg385263
hg195263
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17387049
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5932147
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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