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nsv5891784

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:399

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 147 SVs from 29 studies. See in: genome view    
Submitted genomic179,683,309-179,683,707Question Mark
Overlapping variant regions from other studies: 147 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):179,110,310-179,110,708Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5891784Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5179,683,309179,683,707
nsv5891784RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5179,110,310179,110,708

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17429382duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17429382Submitted genomicNC_000005.10:g.179
683309_179683707du
p
GRCh38 (hg38)NC_000005.10Chr5179,683,309179,683,707
nssv17429382RemappedPerfectNC_000005.9:g.1791
10310_179110708dup
GRCh37.p13First PassNC_000005.9Chr5179,110,310179,110,708

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)
nssv174293820.00241724
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