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nsv6110725

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 123 SVs from 27 studies. See in: genome view    
Submitted genomic35,527,492-35,527,492Question Mark
Overlapping variant regions from other studies: 123 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):36,018,394-36,018,394Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6110725Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1935,527,49235,527,492
nsv6110725RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1936,018,39436,018,394

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17622633insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17622633Submitted genomicNC_000019.10:g.355
27492_35527493ins5
3
GRCh38 (hg38)NC_000019.10Chr1935,527,49235,527,492
nssv17622633RemappedPerfectNC_000019.9:g.3601
8394_36018395ins53
GRCh37.p13First PassNC_000019.9Chr1936,018,39436,018,394

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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