A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5939751



Internal ID22715149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26195350..26213666hg38UCSC Ensembl
chr18:23775314..23793630hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3818317
hg1918317
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17374763
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5939751
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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