nsv821615

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,492

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 42 SVs from 14 studies. See in: genome view    
Remapped(Score: Perfect):7,583,381-7,587,872Question Mark
Overlapping variant regions from other studies: 42 SVs from 14 studies. See in: genome view    
Remapped(Score: Perfect):7,648,267-7,652,758Question Mark
Overlapping variant regions from other studies: 36 SVs from 8 studies. See in: genome view    
Submitted genomic7,554,267-7,558,758Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv821615RemappedPerfectGRCh38 (hg38)Primary AssemblyFirst PassNC_000019.10Chr197,583,3817,587,872
nsv821615RemappedPerfectGRCh37 (hg19)Primary AssemblyFirst PassNC_000019.9Chr197,648,2677,652,758
nsv821615Submitted genomicNCBI36 (hg18)NC_000019.8Chr197,554,2677,558,758

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls from this Sample
nssv1420034deletionNA10851SequencingRead depth1,299

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nssv1420034RemappedPerfectNC_000019.10:g.(?_7583381)_(7587872_?)delGRCh38 (hg38)Primary AssemblyFirst PassNC_000019.10Chr197,583,3817,587,872
nssv1420034RemappedPerfectNC_000019.9:g.(?_7648267)_(7652758_?)delGRCh37 (hg19)Primary AssemblyFirst PassNC_000019.9Chr197,648,2677,652,758
nssv1420034Submitted genomicNC_000019.8:g.(?_7554267)_(7558758_?)delNCBI36 (hg18)NC_000019.8Chr197,554,2677,558,758

There are no validations for this variant

There are no clinical assertions for this variant

There is no genotype information for this variant