A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5980254



Internal ID22755189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:36092776..36092776hg38UCSC Ensembl
chr14:36561982..36561982hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17377509
Samples
Known GenesLINC00609
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5980254
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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