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nsv5446950

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:68

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 83 SVs from 17 studies. See in: genome view    
Submitted genomic231,153,282-231,153,349Question Mark
Overlapping variant regions from other studies: 83 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):232,017,996-232,018,063Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5446950Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2231,153,282231,153,349
nsv5446950RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2232,017,996232,018,063

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17730088deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17730088Submitted genomicNC_000002.12:g.231
153282_231153349de
l
GRCh38 (hg38)NC_000002.12Chr2231,153,282231,153,349
nssv17730088RemappedPerfectNC_000002.11:g.232
017996_232018063de
l
GRCh37.p13First PassNC_000002.11Chr2232,017,996232,018,063

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)
nssv17730088<0.00126404
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