A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17127891



Internal ID21487761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:8952899..9455287hg38UCSC Ensembl
chr4:8954625..9457013hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38502389
hg19502389
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5667406
Supporting Variants
SamplesNA18534
Known GenesDEFB131, USP17L10, USP17L11, USP17L12, USP17L13, USP17L15, USP17L17, USP17L18, USP17L19, USP17L20, USP17L21, USP17L22, USP17L24, USP17L25, USP17L26, USP17L27, USP17L28, USP17L29, USP17L30, USP17L5, USP17L6P, USP17L9P
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17127891
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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