A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829099



Internal ID22604034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:207380118..207392943hg38UCSC Ensembl
chr1:207553463..207566288hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3812826
hg1912826
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456106
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829099
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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