A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5827875



Internal ID22602810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:101361232..101372343hg38UCSC Ensembl
chr1:101826788..101837899hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg3811112
hg1911112
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455446
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5827875
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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