A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17141549



Internal ID21452394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:139251281..139251281hg38UCSC Ensembl
chr6:139572418..139572418hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38524
hg19524
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5638551
Supporting Variants
SamplesHG01596
Known GenesTXLNB
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17141549
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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