A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4752658



Internal ID20528518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5985276..5985276hg38UCSC Ensembl
chr10:6027239..6027239hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16287919
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4752658
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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