A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438578



Internal ID21096131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2050166..2083344hg38UCSC Ensembl
chr11:2071396..2104574hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3833179
hg1933179
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188985
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438578
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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