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nsv5729145

  • Variant Calls:2
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1
  • Description:Insertion of a L1 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: 317 SVs from 34 studies. See in: genome view    
Submitted genomic99,304,071-99,304,071Question Mark
Overlapping variant regions from other studies: 317 SVs from 34 studies. See in: genome view    
Remapped(Score: Perfect):99,844,276-99,844,276Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5729145Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1599,304,07199,304,071
nsv5729145RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1599,844,27699,844,276

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17249332line1 insertionSequencingOther
nssv17251273line1 insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17249332Submitted genomicNC_000015.10:g.993
04071_99304072ins?
GRCh38 (hg38)NC_000015.10Chr1599,304,07199,304,071
nssv17251273Submitted genomicNC_000015.10:g.993
04071_99304072ins?
GRCh38 (hg38)NC_000015.10Chr1599,304,07199,304,071
nssv17249332RemappedPerfectNC_000015.9:g.9984
4276_99844277ins?
GRCh37.p13First PassNC_000015.9Chr1599,844,27699,844,276
nssv17251273RemappedPerfectNC_000015.9:g.9984
4276_99844277ins?
GRCh37.p13First PassNC_000015.9Chr1599,844,27699,844,276

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.

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