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nsv3286099

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:85
  • Description:Sequences at least 70% masked by tandem repeat finder or contained within a tandem repeat
  • Publication(s):Chaisson et al. 2019

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 172 SVs from 41 studies. See in: genome view    
Submitted genomic135,797,422-135,797,506Question Mark
Overlapping variant regions from other studies: 172 SVs from 41 studies. See in: genome view    
Remapped(Score: Perfect):135,482,170-135,482,254Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv3286099Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7135,797,422135,797,506
nsv3286099RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7135,482,170135,482,254

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv14467590deletionSAMN00006581Optical mapping, SequencingOptical mapping, Sequence alignment, de novo and local sequence assembly41,185

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv14467590Submitted genomicNC_000007.14:g.135
797422_135797506de
l84
GRCh38 (hg38)NC_000007.14Chr7135,797,422135,797,506
nssv14467590RemappedPerfectNC_000007.13:g.135
482170_135482254de
l84
GRCh37.p13First PassNC_000007.13Chr7135,482,170135,482,254

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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