A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517441



Internal ID20890802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:62869972..62892168hg38UCSC Ensembl
chr18:60537205..60559401hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3822197
hg1922197
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182661
Samples
Known GenesPHLPP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517441
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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