A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17085951



Internal ID21473425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:42799784..42800554hg38UCSC Ensembl
chr12:43193586..43194356hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg38771
hg19771
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5603397
Supporting Variants
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17085951
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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