A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563227



Internal ID20936298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:17073635..17074365hg38UCSC Ensembl
chr5:17073744..17074474hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38731
hg19731
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267630
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563227
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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