A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17386207



Internal ID22444077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32066067..32066067hg38UCSC Ensembl
chr1:32531668..32531668hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38216
hg19216
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5957017
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17386207
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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