A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18246207



Internal ID20813247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:20546381..23697523hg38UCSC Ensembl
chr19:20729187..23880325hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg383151143
hg193151139
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6595620
Supporting Variants
Samples
Known GenesLINC00664, LOC100132815, LOC100996349, LOC440518, LOC641367, ZNF100, ZNF208, ZNF257, ZNF429, ZNF43, ZNF430, ZNF431, ZNF492, ZNF493, ZNF626, ZNF675, ZNF676, ZNF708, ZNF714, ZNF724P, ZNF728, ZNF729, ZNF730, ZNF737, ZNF738, ZNF85, ZNF91, ZNF98, ZNF99
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18246207
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer