A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17145163



Internal ID21453121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:14212280..14212280hg38UCSC Ensembl
chr7:14251905..14251905hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg38413
hg19413
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5641090
Supporting Variants
SamplesHG02011
Known GenesDGKB
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17145163
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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