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nsv4061733

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:116,750

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 132 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):153,093,077-153,209,826Question Mark
Overlapping variant regions from other studies: 135 SVs from 18 studies. See in: genome view    
Submitted genomic153,065,553-153,182,302Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4061733RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1153,093,077153,209,826
nsv4061733Submitted genomicGRCh37.p13Primary AssemblyNC_000001.10Chr1153,065,553153,182,302

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15854412deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15854412RemappedPerfectNC_000001.11:g.153
093077_153209826de
l
GRCh38.p12First PassNC_000001.11Chr1153,093,077153,209,826
nssv15854412Submitted genomicNC_000001.10:g.153
065553_153182302de
l
GRCh37.p13NC_000001.10Chr1153,065,553153,182,302

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)
nssv158544124.6e-005121694
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