A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17140923



Internal ID21406214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107953778..107953875hg38UCSC Ensembl
chr6:108274982..108275079hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5573048
Supporting Variants
SamplesHG00512
Known GenesSEC63
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17140923
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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