A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551016



Internal ID20924156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:175967321..175967917hg38UCSC Ensembl
chr1:175936457..175937053hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg38597
hg19597
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248770
Samples
Known GenesRFWD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551016
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