A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605479



Internal ID20978550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:111193726..111194592hg38UCSC Ensembl
chr6:111514929..111515795hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38867
hg19867
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18135398
Samples
Known GenesSLC16A10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605479
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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