A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456655



Internal ID21114208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118020408..118021115hg38UCSC Ensembl
chr11:117891123..117891830hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38708
hg19708
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987175
Samples
Known GenesTMPRSS4-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456655
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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