A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17098796



Internal ID21492937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:73074381..73074381hg38UCSC Ensembl
chr13:73648519..73648519hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5655748
Supporting Variants
SamplesNA19238
Known GenesKLF5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17098796
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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