A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17131706



Internal ID21401184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:32604063..32604130hg38UCSC Ensembl
chr5:32604169..32604236hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5574218
Supporting Variants
SamplesHG00096
Known GenesSUB1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17131706
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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