A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562819



Internal ID20935890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:152214362..152215597hg38UCSC Ensembl
chr4:153135514..153136749hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg381236
hg191236
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263855
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562819
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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