A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17079811



Internal ID21490065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110677368..110677368hg38UCSC Ensembl
chr13:111329715..111329715hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5646451
Supporting Variants
SamplesNA19238
Known GenesCARS2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17079811
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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