A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506508



Internal ID20879789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:82574457..82800431hg38UCSC Ensembl
chr15:83243207..83469183hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38225975
hg19225977
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189418
Samples
Known GenesAP3B2, CPEB1, FSD2, LOC283692, LOC283693, LOC338963, SCARNA15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506508
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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