A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440944



Internal ID21098497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:13020447..13049848hg38UCSC Ensembl
chr11:13041994..13071395hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3829402
hg1929402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180343
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440944
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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