A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17138258



Internal ID21509862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:12887563..12887563hg38UCSC Ensembl
chr4:12889187..12889187hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg38435
hg19435
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5605795
Supporting Variants
SamplesNA20847
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17138258
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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