A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504925



Internal ID20878189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66395823..66407394hg38UCSC Ensembl
chr15:66688161..66699732hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3811572
hg1911572
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184348
Samples
Known GenesMAP2K1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504925
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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