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nsv4208989

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,558,965

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1793 SVs from 21 studies. See in: genome view    
Remapped(Score: Good):121,962,383-124,521,347Question Mark
Overlapping variant regions from other studies: 1696 SVs from 21 studies. See in: genome view    
Submitted genomic123,721,898-126,209,916Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4208989RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000010.11Chr10121,962,383124,521,347
nsv4208989Submitted genomicGRCh37.p13Primary AssemblyNC_000010.10Chr10123,721,898126,209,916

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15800105deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15800105RemappedGoodNC_000010.11:g.121
962383_124521347de
l
GRCh38.p12First PassNC_000010.11Chr10121,962,383124,521,347
nssv15800105Submitted genomicNC_000010.10:g.123
721898_126209916de
l
GRCh37.p13NC_000010.10Chr10123,721,898126,209,916

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)
nssv158001054.6e-005121694
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