A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556751



Internal ID20929822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:87922755..87928308hg38UCSC Ensembl
chr5:87218572..87224125hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg385554
hg195554
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269709
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556751
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer