A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4762999



Internal ID20538859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:148738138..148738138hg38UCSC Ensembl
chr6:149059274..149059274hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg382932
hg192932
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16261132
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4762999
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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