A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17108497



Internal ID21487294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:13002471..13002526hg38UCSC Ensembl
chr2:13142596..13142651hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5566874
Supporting Variants
SamplesNA18534
Known GenesLOC100506474
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17108497
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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