A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17139720



Internal ID21403748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:52740609..52740609hg38UCSC Ensembl
chr7:52808303..52808303hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5635146
Supporting Variants
SamplesHG00171
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17139720
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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