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nsv6145338

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:413,161

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2480 SVs from 92 studies. See in: genome view    
Submitted genomic46,291,980-46,705,140Question Mark
Overlapping variant regions from other studies: 2539 SVs from 92 studies. See in: genome view    
Remapped(Score: Perfect):44,369,346-44,782,506Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6145338Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1746,291,98046,705,140
nsv6145338RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1744,369,34644,782,506

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17713435duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17713435Submitted genomicNC_000017.11:g.462
91980_46705140dup
GRCh38 (hg38)NC_000017.11Chr1746,291,98046,705,140
nssv17713435RemappedPerfectNC_000017.10:g.443
69346_44782506dup
GRCh37.p13First PassNC_000017.10Chr1744,369,34644,782,506

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)
nssv177134350.1124474000
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