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nsv5495835

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:119

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 82 SVs from 15 studies. See in: genome view    
Submitted genomic64,993,246-64,993,364Question Mark
Overlapping variant regions from other studies: 82 SVs from 15 studies. See in: genome view    
Remapped(Score: Perfect):65,459,964-65,460,082Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5495835Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1464,993,24664,993,364
nsv5495835RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1465,459,96465,460,082

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17696757deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17696757Submitted genomicNC_000014.9:g.6499
3246_64993364del
GRCh38 (hg38)NC_000014.9Chr1464,993,24664,993,364
nssv17696757RemappedPerfectNC_000014.8:g.6545
9964_65460082del
GRCh37.p13First PassNC_000014.8Chr1465,459,96465,460,082

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)
nssv17696757<0.00126404
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