A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6618734



Internal ID20991805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:130378300..130378631hg38UCSC Ensembl
chr6:130699445..130699776hg19UCSC Ensembl
Cytoband6q23.1
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215550
Samples
Known GenesTMEM200A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6618734
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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