A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845055



Internal ID22619990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169702204..169704679hg38UCSC Ensembl
chr6:170102300..170104775hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg382476
hg192476
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17502294
Samples
Known GenesC6orf120, PHF10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845055
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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