A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863560



Internal ID22638495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:6546622..6557781hg38UCSC Ensembl
chr8:6404143..6415302hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3811160
hg1911160
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509689
Samples
Known GenesANGPT2, MCPH1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863560
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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