A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497677



Internal ID20870885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64426603..64427103hg38UCSC Ensembl
chr15:64718802..64719302hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185182
Samples
Known GenesTRIP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497677
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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