A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521405



Internal ID20894766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26132901..26137700hg38UCSC Ensembl
chr18:23712865..23717664hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg384800
hg194800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191688
Samples
Known GenesPSMA8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521405
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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