A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608147



Internal ID20981218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:150814976..150822095hg38UCSC Ensembl
chr6:151136112..151143231hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg387120
hg197120
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217106
Samples
Known GenesPLEKHG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608147
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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