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nsv5446377

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:320

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 103 SVs from 21 studies. See in: genome view    
Submitted genomic213,005,125-213,005,444Question Mark
Overlapping variant regions from other studies: 103 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):213,869,849-213,870,168Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5446377Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2213,005,125213,005,444
nsv5446377RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2213,869,849213,870,168

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16923744deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16923744Submitted genomicNC_000002.12:g.213
005125_213005444de
l
GRCh38 (hg38)NC_000002.12Chr2213,005,125213,005,444
nssv16923744RemappedPerfectNC_000002.11:g.213
869849_213870168de
l
GRCh37.p13First PassNC_000002.11Chr2213,869,849213,870,168

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)
nssv16923744<0.00136404
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