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nsv4870713

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:305

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 215 SVs from 28 studies. See in: genome view    
Submitted genomic167,117,409-167,117,713Question Mark
Overlapping variant regions from other studies: 215 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):167,530,897-167,531,201Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4870713Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6167,117,409167,117,713
nsv4870713RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6167,530,897167,531,201

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16484817alu deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16484817Submitted genomicNC_000006.12:g.167
117409_167117713de
l
GRCh38 (hg38)NC_000006.12Chr6167,117,409167,117,713
nssv16484817RemappedPerfectNC_000006.11:g.167
530897_167531201de
l
GRCh37.p13First PassNC_000006.11Chr6167,530,897167,531,201

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv16484817<0.0011429246
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