A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5936134



Internal ID22711485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1682259..1687918hg38UCSC Ensembl
chr19:1682258..1687917hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg385660
hg195660
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17391429
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5936134
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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