A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464205



Internal ID21121758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:58480715..58492583hg38UCSC Ensembl
chr11:58248188..58260056hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3811869
hg1911869
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190838
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464205
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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