A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5570840



Internal ID21519210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:206172686..206172778hg38UCSC Ensembl
chr2:207037410..207037502hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17109985
SamplesNA20847
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5570840
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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