A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610726



Internal ID20983797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:165645242..165663825hg38UCSC Ensembl
chr6:166058730..166077313hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3818584
hg1918584
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18142413
Samples
Known GenesPDE10A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610726
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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