A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845351



Internal ID22620286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:69245813..69249487hg38UCSC Ensembl
chr6:69955705..69959379hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg383675
hg193675
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17507920
Samples
Known GenesBAI3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845351
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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