nsv5447726

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:313

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 153 SVs from 36 studies. See in: genome view    
Submitted genomic169,029,726-169,030,038Question Mark
Overlapping variant regions from other studies: 153 SVs from 36 studies. See in: genome view    
Remapped(Score: Perfect):169,886,236-169,886,548Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5447726Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2169,029,726169,030,038
nsv5447726RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2169,886,236169,886,548

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16921866deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16921866Submitted genomicNC_000002.12:g.169
029726_169030038de
l
GRCh38 (hg38)NC_000002.12Chr2169,029,726169,030,038
nssv16921866RemappedPerfectNC_000002.11:g.169
886236_169886548de
l
GRCh37.p13First PassNC_000002.11Chr2169,886,236169,886,548

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)
nssv169218660.1489476404
Support Center