A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863878



Internal ID22638813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75415882..75427168hg38UCSC Ensembl
chr7:75045160..75056450hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3811287
hg1911291
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17502809
Samples
Known GenesNSUN5P1, POM121C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863878
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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