A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4751005



Internal ID20526865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:64239079..64239079hg38UCSC Ensembl
chr1:64704762..64704762hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285243
Samples
Known GenesUBE2U
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4751005
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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