A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473638



Internal ID21131191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:57506240..57508161hg38UCSC Ensembl
chr11:57273713..57275634hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg381922
hg191922
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993434
Samples
Known GenesSLC43A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473638
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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