A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17155487



Internal ID21480002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108523978..108523978hg38UCSC Ensembl
chr6:108845181..108845181hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5642946
Supporting Variants
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17155487
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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