A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559421



Internal ID20932492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:29614277..29615855hg38UCSC Ensembl
chr7:29653893..29655471hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg381579
hg191579
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6631n223
Supporting Variantsnssv18273446
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559421
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