A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17140164



Internal ID21419017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157039670..157039670hg38UCSC Ensembl
chr6:157360804..157360804hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5637229
Supporting Variants
SamplesHG00731
Known GenesARID1B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17140164
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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