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nsv5484680

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:176

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 190 SVs from 40 studies. See in: genome view    
Submitted genomic50,076,707-50,076,882Question Mark
Overlapping variant regions from other studies: 30 SVs from 15 studies. See in: genome view    
Remapped(Score: Perfect):255,882-256,057Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5484680Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1050,076,70750,076,882
nsv5484680RemappedPerfectGRCh37.p13PATCHESFirst PassNW_004504302.1Chr10|NW_0
04504302.1
255,882256,057

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17034661duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17034661Submitted genomicNC_000010.11:g.500
76707_50076882dup
GRCh38 (hg38)NC_000010.11Chr1050,076,70750,076,882
nssv17034661RemappedPerfectNW_004504302.1:g.2
55882_256057dup
GRCh37.p13First PassNW_004504302.1Chr10|NW_0
04504302.1
255,882256,057

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)
nssv170346610.0311746350
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