A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17139134



Internal ID21497123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:149094475..149094475hg38UCSC Ensembl
chr3:148812262..148812262hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38460
hg19460
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5608429
Supporting Variants
SamplesNA19238
Known GenesHLTF-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17139134
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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