A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4751349



Internal ID20527210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:58621959..58621959hg38UCSC Ensembl
chr10:60381719..60381719hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16282941
Samples
Known GenesBICC1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4751349
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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