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nsv5445351

  • 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: 307 SVs from 31 studies. See in: genome view    
Submitted genomic241,662,749-241,662,843Question Mark
Overlapping variant regions from other studies: 307 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):242,602,164-242,602,258Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5445351Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2241,662,749241,662,843
nsv5445351RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2242,602,164242,602,258

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16928825deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16928825Submitted genomicNC_000002.12:g.241
662749_241662843de
l
GRCh38 (hg38)NC_000002.12Chr2241,662,749241,662,843
nssv16928825RemappedPerfectNC_000002.11:g.242
602164_242602258de
l
GRCh37.p13First PassNC_000002.11Chr2242,602,164242,602,258

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)
nssv16928825<0.00116404
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