A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17131422



Internal ID21448135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:175901505..175902454hg38UCSC Ensembl
chr5:175328508..175329457hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38950
hg19950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5574227
Supporting Variants
SamplesHG00733
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17131422
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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