A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4748892



Internal ID20524919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:76183302..76186912hg38UCSC Ensembl
chr2:76410428..76414038hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg383611
hg193611
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16280485
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4748892
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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