A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829954



Internal ID22604889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:248921567..248936325hg38UCSC Ensembl
chr1:249215766..249230524hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3814759
hg1914759
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455537
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829954
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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