A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739320



Internal ID20515293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1489226..1489290hg38UCSC Ensembl
chr10:1531421..1531485hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16274374
Samples
Known GenesADARB2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739320
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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