A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17109986



Internal ID21448982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:206172904..206173036hg38UCSC Ensembl
chr2:207037628..207037760hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5582640
Supporting Variants
SamplesHG00864
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17109986
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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