A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17150575



Internal ID21488560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:138329604..138329604hg38UCSC Ensembl
chr6:138650741..138650741hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg381048
hg191048
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5633999
Supporting Variants
SamplesNA18939
Known GenesKIAA1244
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17150575
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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