A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6086329



Internal ID21995562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7442720..7442720hg38UCSC Ensembl
chr11:7463951..7463951hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382630
hg192630
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17581421
Samples
Known GenesLOC100506258, SYT9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6086329
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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