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nsv3233260

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,106
  • Description:Absence of a L1HS mobile element insertion that is present in the reference
  • Publication(s):Chaisson et al. 2019

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 238 SVs from 64 studies. See in: genome view    
Submitted genomic218,009,143-218,015,248Question Mark
Overlapping variant regions from other studies: 244 SVs from 64 studies. See in: genome view    
Remapped(Score: Perfect):218,182,485-218,188,590Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv3233260Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1218,009,143218,015,248
nsv3233260RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1218,182,485218,188,590

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv14433256line1 deletionHG00514Optical mapping, SequencingOptical mapping, Sequence alignment, de novo and local sequence assembly39,861

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv14433256Submitted genomicNC_000001.11:g.218
009143_218015248de
l6105
GRCh38 (hg38)NC_000001.11Chr1218,009,143218,015,248
nssv14433256RemappedPerfectNC_000001.10:g.218
182485_218188590de
l6105
GRCh37.p13First PassNC_000001.10Chr1218,182,485218,188,590

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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