A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828803



Internal ID22603738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:192753874..192755073hg38UCSC Ensembl
chr1:192723004..192724203hg19UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17460874, nssv17461922
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828803
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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