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nsv6181670

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:301

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 261 SVs from 44 studies. See in: genome view    
Submitted genomic131,289,493-131,289,793Question Mark
Overlapping variant regions from other studies: 261 SVs from 44 studies. See in: genome view    
Remapped(Score: Perfect):133,087,756-133,088,056Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6181670Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10131,289,493131,289,793
nsv6181670RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10133,087,756133,088,056

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17901812deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17901812Submitted genomicNC_000010.11:g.131
289493_131289793de
l
GRCh38 (hg38)NC_000010.11Chr10131,289,493131,289,793
nssv17901812RemappedPerfectNC_000010.10:g.133
087756_133088056de
l
GRCh37.p13First PassNC_000010.10Chr10133,087,756133,088,056

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)
nssv179018120.005112254
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