A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527471



Internal ID20900832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8007410..8150022hg38UCSC Ensembl
chr19:8072294..8214906hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38142613
hg19142613
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199043
Samples
Known GenesCCL25, FBN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527471
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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