A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6063767



Internal ID21973000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:125770905..125770905hg38UCSC Ensembl
chr6:126092051..126092051hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17572683
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6063767
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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