A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5939558



Internal ID22714953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:13778447..13782437hg38UCSC Ensembl
chr18:13778446..13782436hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg383991
hg193991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17373291
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5939558
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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