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nsv5563127

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:53

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 139 SVs from 16 studies. See in: genome view    
Submitted genomic97,730,302-97,730,354Question Mark
Overlapping variant regions from other studies: 139 SVs from 16 studies. See in: genome view    
Remapped(Score: Perfect):98,742,530-98,742,582Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5563127Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr897,730,30297,730,354
nsv5563127RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr898,742,53098,742,582

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17014676sva insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17014676Submitted genomicNC_000008.11:g.977
30302_97730354ins1
240
GRCh38 (hg38)NC_000008.11Chr897,730,30297,730,354
nssv17014676RemappedPerfectNC_000008.10:g.987
42530_98742582ins1
240
GRCh37.p13First PassNC_000008.10Chr898,742,53098,742,582

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)
nssv17014676<0.00116404
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