A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841269



Internal ID22616204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:122006759..122007808hg38UCSC Ensembl
chr5:121342454..121343503hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg381050
hg191050
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17500010
Samples
Known GenesSRFBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841269
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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