A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499416



Internal ID20872635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49546301..49552300hg38UCSC Ensembl
chr15:49838498..49844497hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg386000
hg196000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193303
Samples
Known GenesFAM227B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499416
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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