A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17152216



Internal ID21494969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:147909570..147909570hg38UCSC Ensembl
chr6:148230706..148230706hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5643959
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17152216
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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