A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849549



Internal ID22624484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:135866907..135868098hg38UCSC Ensembl
chr8:136879150..136880341hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg381192
hg191192
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17506925, nssv17506926
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849549
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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