A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523839



Internal ID20897200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3575065..3577112hg38UCSC Ensembl
chr18:3575063..3577110hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg382048
hg192048
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194123
Samples
Known GenesDLGAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523839
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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