A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17133652



Internal ID21416175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:138135188..138135247hg38UCSC Ensembl
chr4:139056342..139056401hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5574281
Supporting Variants
SamplesHG00731
Known GenesSLC7A11-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17133652
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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