A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4759835



Internal ID20535695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6242606..6242606hg38UCSC Ensembl
chr10:6284569..6284569hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38285
hg19285
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16278493
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4759835
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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