A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503786



Internal ID20877042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66420370..66487282hg38UCSC Ensembl
chr15:66712708..66779620hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3866913
hg1966913
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025416
Samples
Known GenesMAP2K1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503786
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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