A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739066



Internal ID20515038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:80706865..80707177hg38UCSC Ensembl
chr2:80933990..80934302hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16266326
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739066
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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