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nsv4810783

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:650

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 99 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):145,858,126-145,858,775Question Mark
Overlapping variant regions from other studies: 99 SVs from 19 studies. See in: genome view    
Submitted genomic146,179,262-146,179,911Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4810783RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr6145,858,126145,858,775
nsv4810783Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000006.11Chr6146,179,262146,179,911

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16331974deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16331974RemappedPerfectNC_000006.12:g.145
858126_145858775de
l
GRCh38.p12First PassNC_000006.12Chr6145,858,126145,858,775
nssv16331974Submitted genomicNC_000006.11:g.146
179262_146179911de
l
GRCh37 (hg19)NC_000006.11Chr6146,179,262146,179,911

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv16331974<0.001116834
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