A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17127996



Internal ID21497664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2271569..2271687hg38UCSC Ensembl
chr5:2271683..2271801hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5568351
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17127996
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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