A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866849



Internal ID22641784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:19385478..19389422hg38UCSC Ensembl
chr8:19242989..19246933hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg383945
hg193945
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505090
Samples
Known GenesSH2D4A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866849
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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