A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609272



Internal ID20982343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109144164..109144547hg38UCSC Ensembl
chr6:109465367..109465750hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38384
hg19384
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137031
Samples
Known GenesCEP57L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609272
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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