A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561594



Internal ID20934665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11125325..11126303hg38UCSC Ensembl
chr6:11125558..11126536hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg38979
hg19979
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6057n223
Supporting Variantsnssv18268487
Samples
Known GenesSMIM13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561594
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