A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17093894



Internal ID21501028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:57041272..57041272hg38UCSC Ensembl
chr14:57507990..57507990hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5646652
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17093894
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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