A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468004



Internal ID21125557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:113685135..113690511hg38UCSC Ensembl
chr11:113555857..113561233hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg385377
hg195377
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17986881
Samples
Known GenesTMPRSS5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468004
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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