A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6096829



Internal ID22006062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73250981..73250981hg38UCSC Ensembl
chr11:72962026..72962026hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38878
hg19878
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17596495
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6096829
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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