A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17153238



Internal ID21459904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:17094082..17094082hg38UCSC Ensembl
chr6:17094313..17094313hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5634157
Supporting Variants
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17153238
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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