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nsv5503299

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:64

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 99 SVs from 17 studies. See in: genome view    
Submitted genomic119,652,195-119,652,258Question Mark
Overlapping variant regions from other studies: 99 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):121,411,707-121,411,770Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5503299Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10119,652,195119,652,258
nsv5503299RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10121,411,707121,411,770

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17039336deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17039336Submitted genomicNC_000010.11:g.119
652195_119652258de
l
GRCh38 (hg38)NC_000010.11Chr10119,652,195119,652,258
nssv17039336RemappedPerfectNC_000010.10:g.121
411707_121411770de
l
GRCh37.p13First PassNC_000010.10Chr10121,411,707121,411,770

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)
nssv17039336<0.00126404
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