A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830788



Internal ID22605723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:88035878..88037777hg38UCSC Ensembl
chr1:88501561..88503460hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17481873, nssv17481874
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830788
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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