A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503500



Internal ID20876755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78130432..78138883hg38UCSC Ensembl
chr15:78422774..78431225hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg388452
hg198452
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178435
Samples
Known GenesCIB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503500
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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