A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510008



Internal ID20883321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:50280984..50281816hg38UCSC Ensembl
chr15:50573181..50574013hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38833
hg19833
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180733
Samples
Known GenesGABPB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510008
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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