A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5594481



Internal ID21543080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18265505..18269887hg38UCSC Ensembl
chrUn_gl000212:94257..98639hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg384383
hg194383
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17095474
SamplesNA19650
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5594481
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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