A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594785



Internal ID20967856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47640307..47640717hg38UCSC Ensembl
chr11:47661859..47662269hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38411
hg19411
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221239
Samples
Known GenesMTCH2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594785
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