A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856280



Internal ID22631215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:17135270..17140474hg38UCSC Ensembl
chr8:16992779..16997983hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg385205
hg195205
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17508578
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856280
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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