A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17151806



Internal ID21463621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:48098318..48098318hg38UCSC Ensembl
chr6:48066054..48066054hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5631069
Supporting Variants
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17151806
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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