A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17146466



Internal ID21456958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:84244301..84244747hg38UCSC Ensembl
chr6:84954019..84954465hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg38447
hg19447
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5578542
Supporting Variants
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17146466
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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