A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848127



Internal ID22623062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:124735101..124736800hg38UCSC Ensembl
chr8:125747343..125749042hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2029n209
Supporting Variantsnssv17506208
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848127
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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