A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17113789



Internal ID21480720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:84892073..84892393hg38UCSC Ensembl
chr2:85119197..85119517hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5571178
Supporting Variants
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17113789
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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