U.S. flag

An official website of the United States government

nsv5430048

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:95

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 153 SVs from 40 studies. See in: genome view    
Submitted genomic45,517,817-45,517,911Question Mark
Overlapping variant regions from other studies: 153 SVs from 40 studies. See in: genome view    
Remapped(Score: Perfect):45,983,489-45,983,583Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5430048Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr145,517,81745,517,911
nsv5430048RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr145,983,48945,983,583

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16901816deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16901816Submitted genomicNC_000001.11:g.455
17817_45517911del
GRCh38 (hg38)NC_000001.11Chr145,517,81745,517,911
nssv16901816RemappedPerfectNC_000001.10:g.459
83489_45983583del
GRCh37.p13First PassNC_000001.10Chr145,983,48945,983,583

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)
nssv169018160.50131956378
Support Center