A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571956



Internal ID20945027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110838715..110839049hg38UCSC Ensembl
chr6:111159918..111160252hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267860
Samples
Known GenesAMD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571956
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