A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830094



Internal ID22605029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:54780239..54833397hg38UCSC Ensembl
chr1:55245912..55299070hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg3853159
hg1953159
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17481051
Samples
Known GenesC1orf177, TTC22
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830094
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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