A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863626



Internal ID22638561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:93950187..93967455hg38UCSC Ensembl
chr8:94962415..94979683hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3817269
hg1917269
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17510252
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863626
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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