A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829000



Internal ID22603935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:203439650..203444509hg38UCSC Ensembl
chr1:203408778..203413637hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg384860
hg194860
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17454006
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829000
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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