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nsv3970707

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:17,485

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 830 SVs from 77 studies. See in: genome view    
Submitted genomic617,351-634,835Question Mark
Overlapping variant regions from other studies: 830 SVs from 77 studies. See in: genome view    
Remapped(Score: Perfect):617,466-634,950Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv3970707Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5617,351634,835
nsv3970707RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5617,466634,950

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15216403inversionOptical mappingOptical mapping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv15216403Submitted genomicNC_000005.10:g.(61
7351_?)_(?_634835)
inv
GRCh38 (hg38)NC_000005.10Chr5617,351634,835
nssv15216403RemappedPerfectNC_000005.9:g.(617
466_?)_(?_634950)i
nv
GRCh37.p13First PassNC_000005.9Chr5617,466634,950

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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