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nsv4564807

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 18 SVs from 4 studies. See in: genome view    
Remapped(Score: Perfect):44,392,262-44,392,262Question Mark
Overlapping variant regions from other studies: 18 SVs from 4 studies. See in: genome view    
Submitted genomic44,359,999-44,359,999Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4564807RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr644,392,26244,392,262
nsv4564807Submitted genomicGRCh37.p13Primary AssemblyNC_000006.11Chr644,359,99944,359,999

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16066871sva insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16066871RemappedPerfectNC_000006.12:g.443
92262_44392263ins3
09
GRCh38.p12First PassNC_000006.12Chr644,392,26244,392,262
nssv16066871Submitted genomicNC_000006.11:g.443
59999_44360000ins3
09
GRCh37.p13NC_000006.11Chr644,359,99944,359,999

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv160668714.6e-005121694
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