A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532702



Internal ID20906063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:6006199..6023411hg38UCSC Ensembl
chr18:6006198..6023410hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3817213
hg1917213
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182297
Samples
Known GenesL3MBTL4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532702
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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