A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437433



Internal ID21094986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10916971..10919105hg38UCSC Ensembl
chr11:10938518..10940652hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg382135
hg192135
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177611
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437433
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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