A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970602



Internal ID22745537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:63620897..63620897hg38UCSC Ensembl
chr14:64087615..64087615hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17380012
Samples
Known GenesWDR89
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970602
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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