A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17121981



Internal ID21451817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:155909944..155909944hg38UCSC Ensembl
chr4:156831096..156831096hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg381029
hg191029
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5605880
Supporting Variants
SamplesHG01596
Known GenesTDO2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17121981
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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