A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849332



Internal ID22624267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:135849876..135863504hg38UCSC Ensembl
chr8:136862119..136875747hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg3813629
hg1913629
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17506924
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849332
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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