A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527023



Internal ID20900384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39556174..39743171hg38UCSC Ensembl
chr19:40046814..40233811hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38186998
hg19186998
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198126
Samples
Known GenesCLC, LGALS13, LGALS14, LGALS16, LGALS17A, LOC100129935
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527023
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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