A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17065948



Internal ID21491109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:4682681..4682681hg38UCSC Ensembl
chr1:4742741..4742741hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5615910
Supporting Variants
SamplesNA19238
Known GenesAJAP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17065948
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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