nsv4671143

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:14,330

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 180 SVs from 46 studies. See in: genome view    
Remapped(Score: Perfect):6,374,905-6,389,234Question Mark
Overlapping variant regions from other studies: 180 SVs from 46 studies. See in: genome view    
Submitted genomic6,374,916-6,389,245Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv4671143RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000019.10Chr196,374,9056,389,234
nsv4671143Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000019.9Chr196,374,9166,389,245

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16182829duplicationCuratedCurated

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv16182829RemappedPerfectNC_000019.10:g.(?_
6374905)_(6389234_
?)dup		GRCh38.p12First PassNC_000019.10Chr196,374,9056,389,234
nssv16182829Submitted genomicNC_000019.9:g.(?_6
374916)_(6389245_?
)dup		GRCh37 (hg19)NC_000019.9Chr196,374,9166,389,245

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)
nssv161828290.01916845
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