A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17147974



Internal ID21504017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140706031..140706031hg38UCSC Ensembl
chr7:140405831..140405831hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5634098
Supporting Variants
SamplesNA19239
Known GenesNDUFB2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17147974
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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