A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455558



Internal ID21113111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:8773126..8871568hg38UCSC Ensembl
chr11:8794673..8893115hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3898443
hg1998443
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194333
Samples
Known GenesST5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455558
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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