A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5827824



Internal ID22602759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:118657209..118679562hg38UCSC Ensembl
chr1:119199832..119222185hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg3822354
hg1922354
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456548
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5827824
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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