A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543565



Internal ID20916811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:40728301..40728786hg38UCSC Ensembl
chr1:41193973..41194458hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38486
hg19486
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250949
Samples
Known GenesNFYC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543565
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