A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445816



Internal ID21103369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:13055044..13056330hg38UCSC Ensembl
chr11:13076591..13077877hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg381287
hg191287
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988377
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445816
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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