A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5597353



Internal ID21545965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9036540..9037199hg38UCSC Ensembl
chr18:9036538..9037197hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38660
hg19660
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17103069
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5597353
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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