A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557713



Internal ID20930784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:146823296..146824708hg38UCSC Ensembl
chr6:147144432..147145844hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg381413
hg191413
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273203
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557713
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