A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523790



Internal ID20897151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:42552501..42557100hg38UCSC Ensembl
chr18:40132466..40137065hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg384600
hg194600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183048
Samples
Known GenesLINC00907
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523790
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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