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nsv5499427

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,977

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 116 SVs from 40 studies. See in: genome view    
Submitted genomic71,501,700-71,504,676Question Mark
Overlapping variant regions from other studies: 115 SVs from 40 studies. See in: genome view    
Remapped(Score: Perfect):71,212,746-71,215,722Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5499427Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1171,501,70071,504,676
nsv5499427RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1171,212,74671,215,722

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17046433deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17046433Submitted genomicNC_000011.10:g.715
01700_71504676del
GRCh38 (hg38)NC_000011.10Chr1171,501,70071,504,676
nssv17046433RemappedPerfectNC_000011.9:g.7121
2746_71215722del
GRCh37.p13First PassNC_000011.9Chr1171,212,74671,215,722

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)
nssv170464330.009566404
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