A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513371



Internal ID20886715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:38775200..38818214hg38UCSC Ensembl
chr15:39067401..39110415hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3843015
hg1943015
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193276
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513371
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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