A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829527



Internal ID22604462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:241192058..241198108hg38UCSC Ensembl
chr1:241355358..241361408hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg386051
hg196051
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464593
Samples
Known GenesRGS7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829527
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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