A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511855



Internal ID20885185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64785544..64821992hg38UCSC Ensembl
chr15:65077743..65114191hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3836449
hg1936449
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179013
Samples
Known GenesPIF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511855
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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