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nsv4321864

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,976,879

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 6063 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):46,154,640-51,131,518Question Mark
Overlapping variant regions from other studies: 6063 SVs from 23 studies. See in: genome view    
Submitted genomic46,657,897-51,634,775Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4321864RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000019.10Chr1946,154,64051,131,518
nsv4321864Submitted genomicGRCh37.p13Primary AssemblyNC_000019.9Chr1946,657,89751,634,775

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16090117inversionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16090117RemappedPerfectNC_000019.10:g.461
54640_51131518inv
GRCh38.p12First PassNC_000019.10Chr1946,154,64051,131,518
nssv16090117Submitted genomicNC_000019.9:g.4665
7897_51634775inv
GRCh37.p13NC_000019.9Chr1946,657,89751,634,775

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)
nssv160901174.6e-005121694
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