A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17144851



Internal ID21485989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:113105284..113105284hg38UCSC Ensembl
chr7:112745339..112745339hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5633885
Supporting Variants
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17144851
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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