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nsv5423409

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:80,131

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 346 SVs from 54 studies. See in: genome view    
Submitted genomic86,544,094-86,624,224Question Mark
Overlapping variant regions from other studies: 346 SVs from 54 studies. See in: genome view    
Remapped(Score: Perfect):87,009,777-87,089,907Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5423409Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr186,544,09486,624,224
nsv5423409RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr187,009,77787,089,907

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16905843duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16905843Submitted genomicNC_000001.11:g.865
44094_86624224dup
GRCh38 (hg38)NC_000001.11Chr186,544,09486,624,224
nssv16905843RemappedPerfectNC_000001.10:g.870
09777_87089907dup
GRCh37.p13First PassNC_000001.10Chr187,009,77787,089,907

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)
nssv169058430.002106404
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