A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475256



Internal ID21132809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65949666..65952105hg38UCSC Ensembl
chr11:65717137..65719576hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg382440
hg192440
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193520
Samples
Known GenesTSGA10IP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475256
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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