A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845549



Internal ID22620484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:54446823..54449817hg38UCSC Ensembl
chr6:54311621..54314615hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg382995
hg192995
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17506516
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845549
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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