A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844645



Internal ID22619580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:148865234..148869492hg38UCSC Ensembl
chr6:149186370..149190628hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg384259
hg194259
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17502400
Samples
Known GenesUST
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844645
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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