A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756640



Internal ID20532500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:125770902..125770902hg38UCSC Ensembl
chr6:126092048..126092048hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16276395
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4756640
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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