A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5575768



Internal ID21524200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:16089996..16090187hg38UCSC Ensembl
chr2:16230118..16230309hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38192
hg19192
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17109438
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5575768
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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