A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609029



Internal ID20982100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110319855..110324277hg38UCSC Ensembl
chr6:110641058..110645480hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg384423
hg194423
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136675
Samples
Known GenesMETTL24
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609029
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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