A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533151



Internal ID20906512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26182101..26186200hg38UCSC Ensembl
chr18:23762065..23766164hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg384100
hg194100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039574
Samples
Known GenesPSMA8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533151
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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