A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850629



Internal ID22625564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:127741266..127748470hg38UCSC Ensembl
chr8:128753512..128760716hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg387205
hg197205
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17506815
Samples
Known GenesMYC
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850629
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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