A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854452



Internal ID22629387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75414420..75420493hg38UCSC Ensembl
chr7:75043698..75049776hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg386074
hg196079
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509314
Samples
Known GenesNSUN5P1, POM121C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854452
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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