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nsv5444140

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,033

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 121 SVs from 28 studies. See in: genome view    
Submitted genomic102,134,023-102,139,055Question Mark
Overlapping variant regions from other studies: 121 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):102,750,483-102,755,515Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5444140Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2102,134,023102,139,055
nsv5444140RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2102,750,483102,755,515

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16916404deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16916404Submitted genomicNC_000002.12:g.102
134023_102139055de
l
GRCh38 (hg38)NC_000002.12Chr2102,134,023102,139,055
nssv16916404RemappedPerfectNC_000002.11:g.102
750483_102755515de
l
GRCh37.p13First PassNC_000002.11Chr2102,750,483102,755,515

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)
nssv16916404<0.00126404
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