A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17153890



Internal ID21467920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:152905617..152906603hg38UCSC Ensembl
chr6:153226752..153227738hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg38987
hg19987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5577366
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17153890
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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