A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17146984



Internal ID21504413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:131558478..131558478hg38UCSC Ensembl
chr7:131243237..131243237hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5633701
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17146984
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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