A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110712



Internal ID22019945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:34011407..34011407hg38UCSC Ensembl
chr21:35383708..35383708hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641662
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110712
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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