A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5945773



Internal ID22721254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102218642..102218722hg38UCSC Ensembl
chr14:102684979..102685059hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17372551
Samples
Known GenesWDR20
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5945773
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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