A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511536



Internal ID20884864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:28642501..29119300hg38UCSC Ensembl
chr15:28887647..29411503hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg38476800
hg19523857
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178058
Samples
Known GenesAPBA2, GOLGA6L7P, GOLGA8M, HERC2P9, LOC100289656, LOC646278, WHAMMP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511536
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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