A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505323



Internal ID20878591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:27837092..28079773hg38UCSC Ensembl
chr15:28082238..28324919hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38242682
hg19242682
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179006
Samples
Known GenesOCA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505323
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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