A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830692



Internal ID22605627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:88168366..88170202hg38UCSC Ensembl
chr1:88634049..88635885hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg381837
hg191837
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17481885, nssv17481886
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830692
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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