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nsv5552390

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:49

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 75 SVs from 21 studies. See in: genome view    
Submitted genomic70,277,061-70,277,109Question Mark
Overlapping variant regions from other studies: 75 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):70,123,167-70,123,215Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5552390Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1170,277,06170,277,109
nsv5552390RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1170,123,16770,123,215

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17046424insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17046424Submitted genomicNC_000011.10:g.702
77061_70277109ins5
6
GRCh38 (hg38)NC_000011.10Chr1170,277,06170,277,109
nssv17046424RemappedPerfectNC_000011.9:g.7012
3167_70123215ins56
GRCh37.p13First PassNC_000011.9Chr1170,123,16770,123,215

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)
nssv170464240.0895335990
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