A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550554



Internal ID20923693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:44118114..44118777hg38UCSC Ensembl
chr2:44345253..44345916hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38664
hg19664
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257981
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550554
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