A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17157468



Internal ID21482672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:146571114..146571114hg38UCSC Ensembl
chr6:146892250..146892250hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg38560
hg19560
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5633166
Supporting Variants
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17157468
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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