A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843714



Internal ID22618649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:114346134..114357729hg38UCSC Ensembl
chr6:114667298..114678893hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg3811596
hg1911596
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501081
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843714
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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