A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17113439



Internal ID21404504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:46206643..46206804hg38UCSC Ensembl
chr2:46433782..46433943hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5577985
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17113439
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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