A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504049



Internal ID20877308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77924606..78018356hg38UCSC Ensembl
chr15:78216948..78310698hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3893751
hg1993751
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196412
Samples
Known GenesLOC645752, LOC91450, TBC1D2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504049
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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