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nsv6198562

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:80

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 98 SVs from 29 studies. See in: genome view    
Submitted genomic52,570,900-52,570,979Question Mark
Overlapping variant regions from other studies: 98 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):52,604,812-52,604,891Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6198562Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1652,570,90052,570,979
nsv6198562RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1652,604,81252,604,891

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17930601deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17930601Submitted genomicNC_000016.10:g.525
70900_52570979del
GRCh38 (hg38)NC_000016.10Chr1652,570,90052,570,979
nssv17930601RemappedPerfectNC_000016.9:g.5260
4812_52604891del
GRCh37.p13First PassNC_000016.9Chr1652,604,81252,604,891

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)
nssv17930601<0.00112342
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