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nsv5460593

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:59

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 73 SVs from 13 studies. See in: genome view    
Submitted genomic161,348,390-161,348,448Question Mark
Overlapping variant regions from other studies: 73 SVs from 13 studies. See in: genome view    
Remapped(Score: Perfect):160,775,397-160,775,455Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5460593Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5161,348,390161,348,448
nsv5460593RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5160,775,397160,775,455

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16977462duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16977462Submitted genomicNC_000005.10:g.161
348390_161348448du
p
GRCh38 (hg38)NC_000005.10Chr5161,348,390161,348,448
nssv16977462RemappedPerfectNC_000005.9:g.1607
75397_160775455dup
GRCh37.p13First PassNC_000005.9Chr5160,775,397160,775,455

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)
nssv16977462<0.00116404
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