A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5943049



Internal ID22718493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35881459..35965094hg38UCSC Ensembl
chr14:36350665..36434300hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg3883636
hg1983636
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17379894
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5943049
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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