A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542639



Internal ID20915897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35096390..35097023hg38UCSC Ensembl
chr1:35561991..35562624hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38634
hg19634
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250902
Samples
Known GenesZMYM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542639
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