A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499182



Internal ID20872399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89944292..90294853hg38UCSC Ensembl
chr15:90487524..90838085hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38350562
hg19350562
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190788
Samples
Known GenesCIB1, GDPGP1, IDH2, NGRN, SEMA4B, TTLL13, ZNF710
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499182
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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