A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572995



Internal ID20946066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:79645666..80289021hg38UCSC Ensembl
chr6:80355383..80998738hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38643356
hg19643356
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271680
Samples
Known GenesBCKDHB, C6orf7, ELOVL4, RNY4, SH3BGRL2, TTK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572995
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