A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856887



Internal ID22631822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:47568093..47587640hg38UCSC Ensembl
chr8:48480655..48500202hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg3819548
hg1919548
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17506772
Samples
Known GenesSPIDR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856887
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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