A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5973101



Internal ID22748036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102328370..102328370hg38UCSC Ensembl
chr14:102794707..102794707hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17372391
Samples
Known GenesZNF839
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5973101
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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