A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17159105



Internal ID21427223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:163230732..163230732hg38UCSC Ensembl
chr6:163651764..163651764hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5637600
Supporting Variants
SamplesHG00731
Known GenesPACRG
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17159105
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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