A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513304



Internal ID20886647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75344292..75357660hg38UCSC Ensembl
chr15:75636633..75650001hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3813369
hg1913369
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185259
Samples
Known GenesMAN2C1, MIR631, NEIL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513304
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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