A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17131356



Internal ID21471915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43378046..43378046hg38UCSC Ensembl
chr5:43378148..43378148hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5642104
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17131356
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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