A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563828



Internal ID20936899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151421292..151422792hg38UCSC Ensembl
chr5:150800853..150802353hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg381501
hg191501
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5989n223
Supporting Variantsnssv18268716
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563828
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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