A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547409



Internal ID20920610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:45094814..45095406hg38UCSC Ensembl
chr1:45560486..45561078hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38593
hg19593
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251876
Samples
Known GenesZSWIM5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547409
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