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nsv932784

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,075,971

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 9340 SVs from 121 studies. See in: genome view    
Remapped(Score: Perfect):16,161,539-19,237,509Question Mark
Overlapping variant regions from other studies: 9340 SVs from 121 studies. See in: genome view    
Submitted genomic16,064,853-19,140,822Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nsv932784RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000017.11Chr1716,161,53916,161,53919,237,50919,237,509
nsv932784Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000017.10Chr1716,064,85316,934,73818,231,20919,140,822

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysis
nssv1611800deletion462Oligo aCGHProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv1611800RemappedPerfectNC_000017.11:g.(16
647373_16647373)_(
18859289_18859289)
del
GRCh38.p12First PassNC_000017.11Chr1716,647,37316,647,37318,859,28918,859,289
nssv1611800RemappedPerfectNC_000017.10:g.(16
550687_16703651)_(
18708864_18762602)
del
GRCh37.p13First PassNC_000017.10Chr1716,550,68716,703,65118,708,86418,762,602
nssv1611800Submitted genomicNC_000017.9:g.(164
91412_16644376)_(1
8649589_18703327)d
el
NCBI36 (hg18)NC_000017.9Chr1716,491,41216,644,37618,649,58918,703,327

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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