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nsv832241

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:218,848

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 823 SVs from 63 studies. See in: genome view    
Remapped(Score: Perfect):98,129,035-98,347,882Question Mark
Overlapping variant regions from other studies: 823 SVs from 63 studies. See in: genome view    
Remapped(Score: Perfect):97,999,763-98,218,610Question Mark
Overlapping variant regions from other studies: 36 SVs from 4 studies. See in: genome view    
Submitted genomic97,504,973-97,723,820Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv832241RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1198,129,03598,347,882
nsv832241RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1197,999,76398,218,610
nsv832241Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000011.8Chr1197,504,97397,723,820

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1449438copy number lossBAC aCGHProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv1449438RemappedPerfectNC_000011.10:g.(98
129035_?)_(?_98347
882)del
GRCh38.p12First PassNC_000011.10Chr1198,129,03598,347,882
nssv1449438RemappedPerfectNC_000011.9:g.(979
99763_?)_(?_982186
10)del
GRCh37.p13First PassNC_000011.9Chr1197,999,76398,218,610
nssv1449438Submitted genomicNC_000011.8:g.(975
04973_?)_(?_977238
20)del
NCBI35 (hg17)NC_000011.8Chr1197,504,97397,723,820

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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