A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4734724



Internal ID20510662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15960263..15960582hg38UCSC Ensembl
chr17:15863577..15863896hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288121
Samples
Known GenesADORA2B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4734724
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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