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nsv6155139

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:78

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 190 SVs from 38 studies. See in: genome view    
Submitted genomic188,980,353-188,980,430Question Mark
Overlapping variant regions from other studies: 190 SVs from 38 studies. See in: genome view    
Remapped(Score: Perfect):189,845,079-189,845,156Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6155139Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2188,980,353188,980,430
nsv6155139RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2189,845,079189,845,156

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17861507deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17861507Submitted genomicNC_000002.12:g.188
980353_188980430de
l
GRCh38 (hg38)NC_000002.12Chr2188,980,353188,980,430
nssv17861507RemappedPerfectNC_000002.11:g.189
845079_189845156de
l
GRCh37.p13First PassNC_000002.11Chr2189,845,079189,845,156

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)
nssv178615070.84316376
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