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nsv832367

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:235,324

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 823 SVs from 81 studies. See in: genome view    
Remapped(Score: Perfect):32,910,710-33,146,033Question Mark
Overlapping variant regions from other studies: 823 SVs from 81 studies. See in: genome view    
Remapped(Score: Perfect):33,063,644-33,298,967Question Mark
Overlapping variant regions from other studies: 35 SVs from 5 studies. See in: genome view    
Submitted genomic32,954,911-33,190,234Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv832367RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr1232,910,71033,146,033
nsv832367RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1233,063,64433,298,967
nsv832367Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000012.9Chr1232,954,91133,190,234

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1449757copy number gainBAC aCGHProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv1449757RemappedPerfectNC_000012.12:g.(32
910710_?)_(?_33146
033)dup
GRCh38.p12First PassNC_000012.12Chr1232,910,71033,146,033
nssv1449757RemappedPerfectNC_000012.11:g.(33
063644_?)_(?_33298
967)dup
GRCh37.p13First PassNC_000012.11Chr1233,063,64433,298,967
nssv1449757Submitted genomicNC_000012.9:g.(329
54911_?)_(?_331902
34)dup
NCBI35 (hg17)NC_000012.9Chr1232,954,91133,190,234

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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