A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829588



Internal ID22604523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:243977024..243979423hg38UCSC Ensembl
chr1:244140326..244142725hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458259
Samples
Known GenesLOC339529
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829588
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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