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nsv930463

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:32,693

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2415 SVs from 90 studies. See in: genome view    
Remapped(Score: Good):106,410,444-106,443,136Question Mark
Overlapping variant regions from other studies: 2260 SVs from 90 studies. See in: genome view    
Submitted genomic106,866,357-106,899,047Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nsv930463RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000014.9Chr14106,410,444106,410,444106,443,136106,443,136
nsv930463Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000014.8Chr14106,866,357106,866,414106,898,992106,899,047

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1607660deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv1607660RemappedGoodNC_000014.9:g.(106
410444_106410444)_
(106443136_1064431
36)del		GRCh38.p12First PassNC_000014.9Chr14106,410,444106,410,444106,443,136106,443,136
nssv1607660Submitted genomicNC_000014.8:g.(106
866357_106866414)_
(106898992_1068990
47)del32700		GRCh37 (hg19)NC_000014.8Chr14106,866,357106,866,414106,898,992106,899,047

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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