A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828344



Internal ID22603279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:149838090..149850243hg38UCSC Ensembl
chr1:149809652..149821810hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg3812154
hg1912159
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17451747
Samples
Known GenesHIST2H2AA3, HIST2H2AA4, HIST2H2BC, HIST2H3A, HIST2H3C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828344
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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