U.S. flag

An official website of the United States government

nsv5718154

  • Variant Calls:2
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1
  • Description:Insertion of a SVA mobile element relative to the reference
  • Publication(s):Chuang et al. 2021

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 157 SVs from 31 studies. See in: genome view    
Submitted genomic55,980,891-55,980,891Question Mark
Overlapping variant regions from other studies: 157 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):56,893,450-56,893,450Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5718154Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr855,980,89155,980,891
nsv5718154RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr856,893,45056,893,450

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17245067sva insertionSequencingOther
nssv17246757sva insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17245067Submitted genomicNC_000008.11:g.559
80891_55980892ins1
263
GRCh38 (hg38)NC_000008.11Chr855,980,89155,980,891
nssv17246757Submitted genomicNC_000008.11:g.559
80891_55980892ins1
240
GRCh38 (hg38)NC_000008.11Chr855,980,89155,980,891
nssv17245067RemappedPerfectNC_000008.10:g.568
93450_56893451ins1
263
GRCh37.p13First PassNC_000008.10Chr856,893,45056,893,450
nssv17246757RemappedPerfectNC_000008.10:g.568
93450_56893451ins1
240
GRCh37.p13First PassNC_000008.10Chr856,893,45056,893,450

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

Support Center