A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17135628



Internal ID21462218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:40800483..40801008hg38UCSC Ensembl
chr5:40800585..40801110hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg38526
hg19526
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5565683
Supporting Variants
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17135628
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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