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nsv5603407

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:76

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 151 SVs from 35 studies. See in: genome view    
Submitted genomic130,777,774-130,777,849Question Mark
Overlapping variant regions from other studies: 151 SVs from 35 studies. See in: genome view    
Remapped(Score: Perfect):133,653,161-133,653,236Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5603407Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9130,777,774130,777,849
nsv5603407RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9133,653,161133,653,236

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv17160114deletionSAMN00006579SequencingSequence alignment23,265

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17160114Submitted genomicNC_000009.12:g.130
777774_130777849de
lA
GRCh38 (hg38)NC_000009.12Chr9130,777,774130,777,849
nssv17160114RemappedPerfectNC_000009.11:g.133
653161_133653236de
lA
GRCh37.p13First PassNC_000009.11Chr9133,653,161133,653,236

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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