A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4763005



Internal ID20538865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:226811220..226811220hg38UCSC Ensembl
chr1:226998921..226998921hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16270962
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4763005
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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