A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459206



Internal ID21116759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74190434..74192123hg38UCSC Ensembl
chr11:73901479..73903168hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg381690
hg191690
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993903
Samples
Known GenesPPME1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459206
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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