A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5654317



Internal ID21602622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95921184..95921184hg38UCSC Ensembl
chr14:96387521..96387521hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg383500
hg193500
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17088603
SamplesHG03732
Known GenesLINC00617
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5654317
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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