A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462929



Internal ID21120482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77593364..77604922hg38UCSC Ensembl
chr11:77304409..77315967hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3811559
hg1911559
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187455
Samples
Known GenesAQP11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462929
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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