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nsv4980930

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:59

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 111 SVs from 21 studies. See in: genome view    
Submitted genomic118,581,838-118,581,896Question Mark
Overlapping variant regions from other studies: 106 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):118,452,553-118,452,611Question Mark
Overlapping variant regions from other studies: 8 SVs from 5 studies. See in: genome view    
Remapped(Score: Perfect):207,276-207,334Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4980930Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11118,581,838118,581,896
nsv4980930RemappedPerfectGRCh37.p13Primary AssemblySecond PassNC_000011.9Chr11118,452,553118,452,611
nsv4980930RemappedPerfectGRCh37.p13PATCHESFirst PassNW_003871072.2Chr11|NW_0
03871072.2
207,276207,334

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16530531deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16530531Submitted genomicNC_000011.10:g.118
581838_118581896de
l
GRCh38 (hg38)NC_000011.10Chr11118,581,838118,581,896
nssv16530531RemappedPerfectNW_003871072.2:g.2
07276_207334del
GRCh37.p13First PassNW_003871072.2Chr11|NW_0
03871072.2
207,276207,334
nssv16530531RemappedPerfectNC_000011.9:g.1184
52553_118452611del
GRCh37.p13Second PassNC_000011.9Chr11118,452,553118,452,611

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)
nssv16530531<0.001129246
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