A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5842719



Internal ID22617654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:39177979..39182876hg38UCSC Ensembl
chr5:39178081..39182978hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg384898
hg194898
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17496675
Samples
Known GenesFYB
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5842719
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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