A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548634



Internal ID20921818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:5527846..5529354hg38UCSC Ensembl
chr2:5667978..5669486hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg381509
hg191509
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258224
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548634
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