A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5827599



Internal ID22602529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:110257449..110268421hg38UCSC Ensembl
chr1:110800071..110811043hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3810973
hg1910973
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456140
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5827599
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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