A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17149129



Internal ID21466746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:92432093..92432093hg38UCSC Ensembl
chr7:92061407..92061407hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg38272
hg19272
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5624878
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17149129
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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