A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848232



Internal ID22623167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:59120521..59121540hg38UCSC Ensembl
chr8:60033080..60034099hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg381020
hg191020
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17507490
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848232
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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