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nsv830528

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:214,808

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 432 SVs from 44 studies. See in: genome view    
Remapped(Score: Perfect):158,698,214-158,913,021Question Mark
Overlapping variant regions from other studies: 432 SVs from 44 studies. See in: genome view    
Remapped(Score: Perfect):158,125,222-158,340,029Question Mark
Overlapping variant regions from other studies: 52 SVs from 3 studies. See in: genome view    
Submitted genomic158,057,800-158,272,607Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv830528RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000005.10Chr5158,698,214158,913,021
nsv830528RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5158,125,222158,340,029
nsv830528Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000005.8Chr5158,057,800158,272,607

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1445123copy number gainBAC aCGHProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv1445123RemappedPerfectNC_000005.10:g.(15
8698214_?)_(?_1589
13021)dup
GRCh38.p12First PassNC_000005.10Chr5158,698,214158,913,021
nssv1445123RemappedPerfectNC_000005.9:g.(158
125222_?)_(?_15834
0029)dup
GRCh37.p13First PassNC_000005.9Chr5158,125,222158,340,029
nssv1445123Submitted genomicNC_000005.8:g.(158
057800_?)_(?_15827
2607)dup
NCBI35 (hg17)NC_000005.8Chr5158,057,800158,272,607

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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