A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268649



Internal ID20835689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:147733548..147734286hg38UCSC Ensembl
chr5:147113111..147113849hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38739
hg19739
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6570028
Supporting Variants
Samples
Known GenesJAKMIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268649
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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