A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501566



Internal ID20874801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75563260..75645738hg38UCSC Ensembl
chr15:75855601..75938079hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3882479
hg1982479
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178022
Samples
Known GenesIMP3, PTPN9, SNUPN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501566
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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