A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573065



Internal ID20946136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:56981299..56982440hg38UCSC Ensembl
chr8:57893858..57894999hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg381142
hg191142
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278320
Samples
Known GenesIMPAD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573065
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