A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6099645



Internal ID22008878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35482944..35482944hg38UCSC Ensembl
chr11:35504492..35504492hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg385912
hg195912
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578879
Samples
Known GenesPAMR1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6099645
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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