A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17145027



Internal ID21465309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:83390206..83390206hg38UCSC Ensembl
chr7:83019522..83019522hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5639411
Supporting Variants
SamplesHG03065
Known GenesSEMA3E
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17145027
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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