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nsv5496132

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:313

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 143 SVs from 34 studies. See in: genome view    
Submitted genomic64,246,985-64,247,297Question Mark
Overlapping variant regions from other studies: 143 SVs from 34 studies. See in: genome view    
Remapped(Score: Perfect):64,014,457-64,014,769Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5496132Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1164,246,98564,247,297
nsv5496132RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1164,014,45764,014,769

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17046704duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17046704Submitted genomicNC_000011.10:g.642
46985_64247297dup
GRCh38 (hg38)NC_000011.10Chr1164,246,98564,247,297
nssv17046704RemappedPerfectNC_000011.9:g.6401
4457_64014769dup
GRCh37.p13First PassNC_000011.9Chr1164,014,45764,014,769

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)
nssv17046704<0.00126404
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