A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520146



Internal ID20893507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:39279458..39308589hg38UCSC Ensembl
chr18:36859422..36888553hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3829132
hg1929132
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192349
Samples
Known GenesLINC00669
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520146
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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