A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449253



Internal ID21106806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:27735747..27737794hg38UCSC Ensembl
chr11:27757294..27759341hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg382048
hg192048
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17989830
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449253
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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