A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17148497



Internal ID21445965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25335938..25335938hg38UCSC Ensembl
chr6:25336166..25336166hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5635754
Supporting Variants
SamplesHG00732
Known GenesLRRC16A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17148497
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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