A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531286



Internal ID20904647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:6239213..6350538hg38UCSC Ensembl
chr18:6239212..6350537hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38111326
hg19111326
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195213
Samples
Known GenesL3MBTL4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531286
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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