A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17150664



Internal ID21460904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:119887133..119887133hg38UCSC Ensembl
chr8:120899373..120899373hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5628766
Supporting Variants
SamplesHG02818
Known GenesDEPTOR
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17150664
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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