A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497403



Internal ID20870609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42857534..42984018hg38UCSC Ensembl
chr15:43149732..43276216hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg38126485
hg19126485
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182920
Samples
Known GenesTTBK2, UBR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497403
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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