A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17121038



Internal ID21486929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:11172..11172hg38UCSC Ensembl
chr5:11172..11172hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5634133
Supporting Variants
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17121038
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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