A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5593100



Internal ID21541685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:14897138..14897913hg38UCSC Ensembl
chr18:14897137..14897912hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38776
hg19776
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17101005
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5593100
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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