A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829577



Internal ID22604512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:241416473..241421607hg38UCSC Ensembl
chr1:241579773..241584907hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg385135
hg195135
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17469595
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829577
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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