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nsv5435706

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:162

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 102 SVs from 21 studies. See in: genome view    
Submitted genomic102,887,964-102,888,125Question Mark
Overlapping variant regions from other studies: 102 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):103,504,423-103,504,584Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5435706Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2102,887,964102,888,125
nsv5435706RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2103,504,423103,504,584

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16917058deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16917058Submitted genomicNC_000002.12:g.102
887964_102888125de
l
GRCh38 (hg38)NC_000002.12Chr2102,887,964102,888,125
nssv16917058RemappedPerfectNC_000002.11:g.103
504423_103504584de
l
GRCh37.p13First PassNC_000002.11Chr2103,504,423103,504,584

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)
nssv169170580.01636404
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