A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17142332



Internal ID21454154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170344151..170344326hg38UCSC Ensembl
chr6:170653239..170653414hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5578335
Supporting Variants
SamplesHG02011
Known GenesFAM120B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17142332
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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