A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448985



Internal ID21106538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:25647776..25910915hg38UCSC Ensembl
chr11:25669322..25932462hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38263140
hg19263141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1006n223
Supporting Variantsnssv17990057
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448985
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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