A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4740857



Internal ID20516834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:1929869..1929927hg38UCSC Ensembl
chr12:2039035..2039093hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16279217
Samples
Known GenesLINC00940
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4740857
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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