A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4763453



Internal ID20539313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11491502..11491502hg38UCSC Ensembl
chr6:11491735..11491735hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16278057
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4763453
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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