A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506795



Internal ID20880080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66721402..66725259hg38UCSC Ensembl
chr15:67013740..67017597hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg383858
hg193858
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025430
Samples
Known GenesSMAD6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506795
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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