A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17094276



Internal ID21508572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:34200613..34200946hg38UCSC Ensembl
chr12:34353548..34353881hg19UCSC Ensembl
Cytoband12p11.1
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5602378
Supporting Variants
SamplesNA20509
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17094276
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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