A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552578



Internal ID20925703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:74749781..74750976hg38UCSC Ensembl
chr1:75215465..75216660hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg381196
hg191196
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253114
Samples
Known GenesTYW3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552578
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