A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828564



Internal ID22603499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:179255322..179272967hg38UCSC Ensembl
chr1:179224457..179242102hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3817646
hg1917646
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17449666
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828564
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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