A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17159142



Internal ID21509876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75428820..75428820hg38UCSC Ensembl
chr7:75058102..75058102hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38249
hg19249
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5625487
Supporting Variants
SamplesNA20847
Known GenesPOM121C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17159142
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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