A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17144925



Internal ID21499113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26552810..26552810hg38UCSC Ensembl
chr7:26592429..26592429hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5641634
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17144925
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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