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nsv4773326

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:58

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 128 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):44,776,343-44,776,401Question Mark
Overlapping variant regions from other studies: 128 SVs from 27 studies. See in: genome view    
Submitted genomic45,242,015-45,242,073Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4773326RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr144,776,344 (-1)44,776,401
nsv4773326Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000001.10Chr145,242,016 (-1)45,242,073

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16310301deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16310301RemappedPerfectNC_000001.11:g.(44
776343_?)_44776401
del
GRCh38.p12First PassNC_000001.11Chr144,776,344 (-1)44,776,401
nssv16310301Submitted genomicNC_000001.10:g.(45
242015_?)_45242073
del
GRCh37 (hg19)NC_000001.10Chr145,242,016 (-1)45,242,073

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)
nssv16310301<0.001116834
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