A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496331



Internal ID20869532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66763154..66767584hg38UCSC Ensembl
chr15:67055492..67059922hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg384431
hg194431
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025432
Samples
Known GenesSMAD6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496331
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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