A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4743770



Internal ID20519760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97667490..97673275hg38UCSC Ensembl
chr10:99427247..99433032hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg385786
hg195786
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16272996
Samples
Known GenesPI4K2A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4743770
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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