nsv5514135

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:17,352,001

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 61716 SVs from 132 studies. See in: genome view    
Submitted genomic62,909,528-80,261,528Question Mark
Overlapping variant regions from other studies: 61593 SVs from 132 studies. See in: genome view    
Remapped(Score: Good):60,576,761-78,017,154Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5514135Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1862,909,52880,261,528
nsv5514135RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1860,576,76178,017,154

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17718782deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17718782Submitted genomicNC_000018.10:g.629
09528_80261528del
GRCh38 (hg38)NC_000018.10Chr1862,909,52880,261,528
nssv17718782RemappedGoodNC_000018.9:g.6057
6761_78017154del
GRCh37.p13First PassNC_000018.9Chr1860,576,76178,017,154

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)
nssv17718782<0.00126404
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