A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455385



Internal ID21112938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18112654..18119965hg38UCSC Ensembl
chr11:18134201..18141512hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg387312
hg197312
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988630
Samples
Known GenesSAA3P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455385
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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