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nsv6314476

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: Yes
  • Region Size:1

Genome View

Select assembly:
Overlapping variant regions from other studies: 111 SVs from 38 studies. See in: genome view    
Remapped(Score: Perfect):120,216,282-120,216,282Question Mark
Overlapping variant regions from other studies: 87 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):81,477,505-81,477,505Question Mark
Overlapping variant regions from other studies: 11 SVs from 11 studies. See in: genome view    
Remapped(Score: Perfect):52,099-52,099Question Mark
Overlapping variant regions from other studies: 111 SVs from 38 studies. See in: genome view    
Submitted genomic121,137,437-121,137,437Question Mark
Overlapping variant regions from other studies: 87 SVs from 29 studies. See in: genome view    
Submitted genomic81,106,821-81,106,821Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStopstrand
nsv6314476RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000004.12Chr4120,216,282120,216,282+
nsv6314476RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr781,477,50581,477,505+
nsv6314476RemappedPerfectGRCh38.p12ALT_REF_LOCI_1Second PassNT_187544.1Chr4|NT_18
7544.1
52,09952,099+
nsv6314476Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000004.11Chr4121,137,437121,137,437+
nsv6314476Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr781,106,82181,106,821+

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStopstrand
nssv17975424RemappedPerfectGRCh38.p12Second PassNT_187544.1Chr4|NT_18
7544.1
52,09952,099+
nssv17975424RemappedPerfectGRCh38.p12First PassNC_000004.12Chr4120,216,282120,216,282+
nssv17975424RemappedPerfectGRCh38.p12First PassNC_000007.14Chr781,477,50581,477,505+
nssv17975424Submitted genomicGRCh37 (hg19)NC_000004.11Chr4121,137,437121,137,437+
nssv17975424Submitted genomicGRCh37 (hg19)NC_000007.13Chr781,106,82181,106,821+

No validation data were submitted for this variant

No genotype data were submitted for this variant

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