A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466919



Internal ID21124472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62499508..62506166hg38UCSC Ensembl
chr11:62266980..62273638hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg386659
hg196659
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190110
Samples
Known GenesAHNAK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466919
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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