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nsv6145875

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:455,665

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1105 SVs from 61 studies. See in: genome view    
Submitted genomic52,529,072-52,984,736Question Mark
Overlapping variant regions from other studies: 1105 SVs from 61 studies. See in: genome view    
Remapped(Score: Perfect):52,562,984-53,018,648Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6145875Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1652,529,07252,984,736
nsv6145875RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1652,562,98453,018,648

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17707445duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17707445Submitted genomicNC_000016.10:g.525
29072_52984736dup
GRCh38 (hg38)NC_000016.10Chr1652,529,07252,984,736
nssv17707445RemappedPerfectNC_000016.9:g.5256
2984_53018648dup
GRCh37.p13First PassNC_000016.9Chr1652,562,98453,018,648

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)
nssv17707445<0.00126404
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