A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441861



Internal ID21099414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:28514013..28528528hg38UCSC Ensembl
chr11:28535560..28550075hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3814516
hg1914516
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17990373
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441861
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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