A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829365



Internal ID22604300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:220378558..220379657hg38UCSC Ensembl
chr1:220551900..220552999hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17457283
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829365
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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