A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534103



Internal ID20907464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11889167..11916895hg38UCSC Ensembl
chr18:11889166..11916894hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3827729
hg1927729
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038743
Samples
Known GenesMPPE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534103
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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