A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498688



Internal ID20871901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40792565..40794422hg38UCSC Ensembl
chr15:41084763..41086620hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg381858
hg191858
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193016
Samples
Known GenesDNAJC17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498688
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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