A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830088



Internal ID22605023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:53388493..53393051hg38UCSC Ensembl
chr1:53854165..53858723hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg384559
hg194559
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17480095
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830088
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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