A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5827673



Internal ID22602608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:102925924..102927023hg38UCSC Ensembl
chr1:103391480..103392579hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455142
Samples
Known GenesCOL11A1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5827673
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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