A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4733906



Internal ID20509838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43306128..43388645hg38UCSC Ensembl
chr17:41383490..41466013hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3882518
hg1982524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288847
Samples
Known GenesLINC00910
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4733906
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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