A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830853



Internal ID22605788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:95452138..95453872hg38UCSC Ensembl
chr1:95917694..95919428hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg381735
hg191735
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv50n209
Supporting Variantsnssv17482498, nssv17482497
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830853
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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