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nsv256

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:60,951

Genome View

Select assembly:
Overlapping variant regions from other studies: 402 SVs from 63 studies. See in: genome view    
Remapped(Score: Perfect):49,508,518-49,569,468Question Mark
Overlapping variant regions from other studies: 403 SVs from 64 studies. See in: genome view    
Remapped(Score: Perfect):49,510,535-49,571,485Question Mark
Overlapping variant regions from other studies: 17 SVs from 6 studies. See in: genome view    
Submitted genomic49,351,463-49,412,413Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv256RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000004.12Chr449,508,51849,569,468
nsv256RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr449,510,53549,571,485
nsv256Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000004.9Chr449,351,46349,412,413

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv256inversionSAMN00000376SequencingPaired-end mapping297

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv256RemappedPerfectNC_000004.12:g.(49
508518_?)_(?_49569
468)inv
GRCh38.p12First PassNC_000004.12Chr449,508,51849,569,468
nssv256RemappedPerfectNC_000004.11:g.(49
510535_?)_(?_49571
485)inv
GRCh37.p13First PassNC_000004.11Chr449,510,53549,571,485
nssv256Submitted genomicNC_000004.9:g.(493
51463_?)_(?_494124
13)inv
NCBI35 (hg17)NC_000004.9Chr449,351,46349,412,413

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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