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nsv5466550

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:137,384

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 598 SVs from 63 studies. See in: genome view    
Submitted genomic27,711,907-27,849,290Question Mark
Overlapping variant regions from other studies: 598 SVs from 63 studies. See in: genome view    
Remapped(Score: Good):27,679,686-27,817,068Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5466550Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr627,711,90727,849,290
nsv5466550RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr627,679,68627,817,068

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16980876duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16980876Submitted genomicNC_000006.12:g.277
11907_27849290dup
GRCh38 (hg38)NC_000006.12Chr627,711,90727,849,290
nssv16980876RemappedGoodNC_000006.11:g.276
79686_27817068dup
GRCh37.p13First PassNC_000006.11Chr627,679,68627,817,068

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)
nssv16980876<0.00116404
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