A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17149610



Internal ID21423135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85663245..85664209hg38UCSC Ensembl
chr6:86372963..86373927hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg38965
hg19965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5580102
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17149610
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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