A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607270



Internal ID20980341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110334082..110340723hg38UCSC Ensembl
chr6:110655285..110661926hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg386642
hg196642
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216804
Samples
Known GenesMETTL24
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607270
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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