A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17153909



Internal ID21494691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170079620..170079620hg38UCSC Ensembl
chr6:170394844..170394844hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5628616
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17153909
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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