A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553526



Internal ID20926636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9895519..9896428hg38UCSC Ensembl
chr1:9955577..9956486hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38910
hg19910
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252806
Samples
Known GenesCTNNBIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553526
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