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nsv499527

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,018

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 362 SVs from 46 studies. See in: genome view    
Remapped(Score: Perfect):170,376,907-170,377,924Question Mark
Overlapping variant regions from other studies: 362 SVs from 46 studies. See in: genome view    
Remapped(Score: Perfect):170,685,995-170,687,012Question Mark
Overlapping variant regions from other studies: 195 SVs from 17 studies. See in: genome view    
Submitted genomic170,527,920-170,528,937Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv499527RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr6170,376,907170,377,924
nsv499527RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6170,685,995170,687,012
nsv499527Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000006.10Chr6170,527,920170,528,937

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv585626copy number gainSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv585626RemappedPerfectNC_000006.12:g.170
376907_170377924du
p
GRCh38.p12First PassNC_000006.12Chr6170,376,907170,377,924
nssv585626RemappedPerfectNC_000006.11:g.170
685995_170687012du
p
GRCh37.p13First PassNC_000006.11Chr6170,685,995170,687,012
nssv585626Submitted genomicNC_000006.10:g.170
527920_170528937du
p
NCBI36 (hg18)NC_000006.10Chr6170,527,920170,528,937

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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