A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17146752



Internal ID21475699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41357592..41357592hg38UCSC Ensembl
chr6:41325330..41325330hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38139
hg19139
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5630376
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17146752
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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