U.S. flag

An official website of the United States government

nsv469533

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:101,736

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 579 SVs from 74 studies. See in: genome view    
Remapped(Score: Good):63,645,259-63,746,994Question Mark
Overlapping variant regions from other studies: 455 SVs from 69 studies. See in: genome view    
Remapped(Score: Good):68,240,993-68,342,728Question Mark
Overlapping variant regions from other studies: 6 SVs from 2 studies. See in: genome view    
Submitted genomic64,908,723-65,010,495Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv469533RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr963,645,25963,746,994
nsv469533RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr968,240,99368,342,728
nsv469533Submitted genomicNCBI34 (hg16)Primary AssemblyGPC_000000201.1Chr964,908,72365,010,495

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1675734copy number gainBAC aCGHProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv1675734RemappedGoodNC_000009.12:g.(?_
63645259)_(6374699
4_?)dup
GRCh38.p12First PassNC_000009.12Chr963,645,25963,746,994
nssv1675734RemappedGoodNC_000009.11:g.(?_
68240993)_(6834272
8_?)dup
GRCh37.p13First PassNC_000009.11Chr968,240,99368,342,728
nssv1675734Submitted genomicGPC_000000201.1:g.
(?_64908723)_(6501
0495_?)dup
NCBI34 (hg16)GPC_000000201.1Chr964,908,72365,010,495

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

Support Center