A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473148



Internal ID21130701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:37702550..37703802hg38UCSC Ensembl
chr11:37724100..37725352hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg381253
hg191253
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17990515
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473148
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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