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nsv4525345

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:185,002

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 182 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):34,908,387-35,093,388Question Mark
Overlapping variant regions from other studies: 182 SVs from 17 studies. See in: genome view    
Submitted genomic34,947,999-35,133,000Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4525345RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr734,908,38735,093,388
nsv4525345Submitted genomicGRCh37.p13Primary AssemblyNC_000007.13Chr734,947,99935,133,000

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15980880duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15980880RemappedPerfectNC_000007.14:g.349
08387_35093388dup
GRCh38.p12First PassNC_000007.14Chr734,908,38735,093,388
nssv15980880Submitted genomicNC_000007.13:g.349
47999_35133000dup
GRCh37.p13NC_000007.13Chr734,947,99935,133,000

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)
nssv159808804.6e-005121684
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