A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848026



Internal ID22622961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:95067402..95069701hg38UCSC Ensembl
chr8:96079630..96081929hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17510274
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848026
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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