A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544969



Internal ID20918207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:212732330..212733400hg38UCSC Ensembl
chr1:212905672..212906742hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg381071
hg191071
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248520
Samples
Known GenesNSL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544969
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