A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17377749



Internal ID22435619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:30786693..30796606hg38UCSC Ensembl
chr14:31255899..31265812hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg389914
hg199914
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5932850
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17377749
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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