A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17151402



Internal ID21444190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:161265269..161265269hg38UCSC Ensembl
chr6:161686301..161686301hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5627350
Supporting Variants
SamplesHG00732
Known GenesAGPAT4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17151402
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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